Canonical Allele Identifier: CA360485016

Gene: CAST ERAP1

Linked Data

• dbSNP Id: rs1768291162
• MyVariant Identifiers: chr5:g.96098056G>A (hg19) ; chr5:g.96762352G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.96762352G>A , CM000667.2:g.96762352G>A	GRCh38
NC_000005.9:g.96098056G>A , CM000667.1:g.96098056G>A	GRCh37
NC_000005.8:g.96123812G>A	NCBI36
NG_027839.1:g.56793C>T
NG_029490.1:g.105316G>A
NG_027839.2:g.178632C>T
NG_029490.2:g.105316G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000484552.6:c.832G>A (CAST)	ENSP00000432878.2:p.Ala278Thr
ENST00000508608.6:c.1762G>A (CAST)	ENSP00000422677.2:p.Ala588Thr
ENST00000510756.6:c.1540G>A (CAST)	ENSP00000422176.2:p.Ala514Thr
ENST00000674587.1:c.1369G>A (CAST)	ENSP00000501797.1:p.Ala457Thr
ENST00000674702.1:c.1654G>A (CAST)	ENSP00000502345.1:p.Ala552Thr
ENST00000674984.1:c.1846G>A (CAST)	ENSP00000501713.1:p.Ala616Thr
ENST00000675033.1:c.1540G>A (CAST)	ENSP00000501659.1:p.Ala514Thr
ENST00000675179.1:c.1912G>A (CAST) MANE Select	ENSP00000501872.1:p.Ala638Thr
ENST00000675185.1:c.293G>A (CAST)
ENST00000675266.1:c.1814G>A (CAST)
ENST00000675267.1:c.*1536G>A (CAST)	ENSP00000502095.1:n.*1536G>A
ENST00000675275.1:c.629G>A (CAST)
ENST00000675479.1:c.1525G>A (CAST)	ENSP00000502244.1:p.Ala509Thr
ENST00000675614.1:c.1582G>A (CAST)	ENSP00000502136.1:p.Ala528Thr
ENST00000675663.1:c.1801G>A (CAST)	ENSP00000502449.1:p.Ala601Thr
ENST00000675734.1:n.456G>A (CAST)
ENST00000675858.1:c.1456G>A (CAST)	ENSP00000501780.1:p.Ala486Thr
ENST00000296754.7:c.*848C>T (ERAP1)	ENSP00000296754.3:n.*848C>T
ENST00000309190.9:c.1597G>A (CAST)	ENSP00000312523.5:p.Ala533Thr
ENST00000325674.11:c.832G>A (CAST)	ENSP00000320319.8:p.Ala278Thr
ENST00000338252.7:c.1624G>A (CAST)	ENSP00000343421.3:p.Ala542Thr
ENST00000341926.7:c.1663G>A (CAST)	ENSP00000339914.3:p.Ala555Thr
ENST00000348386.7:n.1605G>A (CAST)
ENST00000395812.6:c.1789G>A (CAST)	ENSP00000379157.2:p.Ala597Thr
ENST00000395813.5:c.1663G>A (CAST)	ENSP00000379158.2:p.Ala555Thr
ENST00000437034.6:c.918G>A (CAST)
ENST00000484552.5:c.890G>A (CAST)
ENST00000504465.5:c.1447G>A (CAST)	ENSP00000425670.1:p.Ala483Thr
ENST00000508579.5:c.808G>A (CAST)	ENSP00000425787.1:p.Ala270Thr
ENST00000508608.5:c.1801G>A (CAST)	ENSP00000422677.1:p.Ala601Thr
ENST00000508830.5:c.1912G>A (CAST)	ENSP00000425721.1:p.Ala638Thr
ENST00000509903.5:c.1558G>A (CAST)	ENSP00000426946.1:p.Ala520Thr
ENST00000510098.1:c.148G>A (CAST)	ENSP00000427195.1:p.Ala50Thr
ENST00000510156.5:c.1663G>A (CAST)	ENSP00000422325.1:p.Ala555Thr
ENST00000510500.5:c.935G>A (CAST)
ENST00000510756.5:c.1846G>A (CAST)	ENSP00000422176.1:p.Ala616Thr
ENST00000511049.5:c.1621G>A (CAST)	ENSP00000421130.1:p.Ala541Thr
ENST00000511782.5:c.1621G>A (CAST)	ENSP00000423638.1:p.Ala541Thr
ENST00000515663.5:c.832G>A (CAST)	ENSP00000422929.1:p.Ala278Thr
NM_001042440.3:c.1789G>A (CAST)	NP_001035905.1:p.Ala597Thr
NM_001190442.1:c.1624G>A (CAST)	NP_001177371.1:p.Ala542Thr
NM_001284212.1:c.1540G>A (CAST)	NP_001271141.1:p.Ala514Thr
NM_001284213.1:c.1447G>A (CAST)	NP_001271142.1:p.Ala483Thr
NM_016442.3:c.*848C>T (ERAP1)	NP_057526.3:n.*848C>T
NM_173060.3:c.1597G>A (CAST)	NP_775083.1:p.Ala533Thr
NR_104285.1:n.919G>A (CAST)
XM_006714696.2:c.1912G>A (CAST)	XP_006714759.1:p.Ala638Thr
XM_006714697.2:c.1912G>A (CAST)	XP_006714760.1:p.Ala638Thr
XM_006714698.2:c.1873G>A (CAST)	XP_006714761.1:p.Ala625Thr
XM_006714699.2:c.1867G>A (CAST)	XP_006714762.1:p.Ala623Thr
XM_006714700.2:c.1855G>A (CAST)	XP_006714763.1:p.Ala619Thr
XM_006714701.2:c.1846G>A (CAST)	XP_006714764.1:p.Ala616Thr
XM_006714702.2:c.1810G>A (CAST)	XP_006714765.1:p.Ala604Thr
XM_006714703.2:c.1807G>A (CAST)	XP_006714766.1:p.Ala603Thr
XM_006714704.2:c.1801G>A (CAST)	XP_006714767.1:p.Ala601Thr
XM_006714705.2:c.1789G>A (CAST)	XP_006714768.1:p.Ala597Thr
XM_006714706.2:c.1744G>A (CAST)	XP_006714769.1:p.Ala582Thr
XM_006714707.2:c.1663G>A (CAST)	XP_006714770.1:p.Ala555Thr
XM_006714708.2:c.1624G>A (CAST)	XP_006714771.1:p.Ala542Thr
XM_006714709.2:c.1606G>A (CAST)	XP_006714772.1:p.Ala536Thr
XM_006714710.2:c.1558G>A (CAST)	XP_006714773.1:p.Ala520Thr
XM_006714711.2:c.1540G>A (CAST)	XP_006714774.1:p.Ala514Thr
XM_006714712.2:c.1501G>A (CAST)	XP_006714775.1:p.Ala501Thr
XM_006714713.2:c.832G>A (CAST)	XP_006714776.1:p.Ala278Thr
XM_006714714.2:c.832G>A (CAST)	XP_006714777.1:p.Ala278Thr
XM_006714715.2:c.808G>A (CAST)	XP_006714778.1:p.Ala270Thr
XM_011543487.1:c.*848C>T (ERAP1)	XP_011541789.1:n.*848C>T
XM_011543654.1:c.1831G>A (CAST)	XP_011541956.1:p.Ala611Thr
XM_011543655.1:c.1828G>A (CAST)	XP_011541957.1:p.Ala610Thr
XM_011543656.1:c.1765G>A (CAST)	XP_011541958.1:p.Ala589Thr
XM_011543657.1:c.1720G>A (CAST)	XP_011541959.1:p.Ala574Thr
XM_011543658.1:c.1516G>A (CAST)	XP_011541960.1:p.Ala506Thr
NM_001042440.4:c.1789G>A (CAST)	NP_001035905.1:p.Ala597Thr
NM_001042441.2:c.1855G>A (CAST)	NP_001035906.1:p.Ala619Thr
NM_001042442.2:c.1846G>A (CAST)	NP_001035907.1:p.Ala616Thr
NM_001042443.2:c.1663G>A (CAST)	NP_001035908.1:p.Ala555Thr
NM_001042444.2:c.1540G>A (CAST)	NP_001035909.1:p.Ala514Thr
NM_001042445.2:c.1558G>A (CAST)	NP_001035910.1:p.Ala520Thr
NM_001042446.2:c.1501G>A (CAST)	NP_001035911.1:p.Ala501Thr
NM_001284212.3:c.1540G>A (CAST)	NP_001271141.1:p.Ala514Thr
NM_001284213.3:c.1447G>A (CAST)	NP_001271142.1:p.Ala483Thr
NM_001330626.1:c.1816G>A (CAST)	NP_001317555.1:p.Ala606Thr
NM_001330627.1:c.1789G>A (CAST)	NP_001317556.1:p.Ala597Thr
NM_001330628.1:c.1744G>A (CAST)	NP_001317557.1:p.Ala582Thr
NM_001330629.1:c.1828G>A (CAST)	NP_001317558.1:p.Ala610Thr
NM_001330630.1:c.1501G>A (CAST)	NP_001317559.1:p.Ala501Thr
NM_001330631.1:c.1624G>A (CAST)	NP_001317560.1:p.Ala542Thr
NM_001330632.1:c.1597G>A (CAST)	NP_001317561.1:p.Ala533Thr
NM_001330633.1:c.1606G>A (CAST)	NP_001317562.1:p.Ala536Thr
NM_001330634.1:c.1567G>A (CAST)	NP_001317563.1:p.Ala523Thr
NM_001349244.1:c.*848C>T (ERAP1)	NP_001336173.1:n.*848C>T
NM_001750.6:c.1912G>A (CAST)	NP_001741.4:p.Ala638Thr
NM_016442.4:c.*848C>T (ERAP1)	NP_057526.3:n.*848C>T
NM_173060.4:c.1597G>A (CAST)	NP_775083.1:p.Ala533Thr
XR_001742119.2:n.3833C>T (ERAP1)
NM_001042440.5:c.1789G>A (CAST)	NP_001035905.1:p.Ala597Thr
NM_001042441.3:c.1855G>A (CAST)	NP_001035906.1:p.Ala619Thr
NM_001042442.3:c.1846G>A (CAST)	NP_001035907.1:p.Ala616Thr
NM_001330626.2:c.1816G>A (CAST)	NP_001317555.1:p.Ala606Thr
NM_001330627.2:c.1789G>A (CAST)	NP_001317556.1:p.Ala597Thr
NM_001330628.2:c.1744G>A (CAST)	NP_001317557.1:p.Ala582Thr
NM_001330629.2:c.1828G>A (CAST)	NP_001317558.1:p.Ala610Thr
NM_001375317.1:c.1801G>A (CAST)	NP_001362246.1:p.Ala601Thr
NM_001750.7:c.1912G>A (CAST) MANE Select	NP_001741.4:p.Ala638Thr
NR_104285.2:n.857G>A (CAST)
NM_001042443.3:c.1663G>A (CAST)	NP_001035908.1:p.Ala555Thr
NM_001042444.3:c.1540G>A (CAST)	NP_001035909.1:p.Ala514Thr
NM_001042445.3:c.1558G>A (CAST)	NP_001035910.1:p.Ala520Thr
NM_001042446.3:c.1501G>A (CAST)	NP_001035911.1:p.Ala501Thr
NM_001190442.2:c.1624G>A (CAST)	NP_001177371.1:p.Ala542Thr
NM_001284212.4:c.1540G>A (CAST)	NP_001271141.1:p.Ala514Thr
NM_001284213.4:c.1447G>A (CAST)	NP_001271142.1:p.Ala483Thr
NM_001330630.2:c.1501G>A (CAST)	NP_001317559.1:p.Ala501Thr
NM_001330631.2:c.1624G>A (CAST)	NP_001317560.1:p.Ala542Thr
NM_001330632.2:c.1597G>A (CAST)	NP_001317561.1:p.Ala533Thr
NM_001330633.2:c.1606G>A (CAST)	NP_001317562.1:p.Ala536Thr
NM_001330634.2:c.1567G>A (CAST)	NP_001317563.1:p.Ala523Thr
NM_001349244.2:c.*848C>T (ERAP1)	NP_001336173.1:n.*848C>T
NM_016442.5:c.*848C>T (ERAP1)	NP_057526.3:n.*848C>T
NM_173060.5:c.1597G>A (CAST)	NP_775083.1:p.Ala533Thr