Canonical Allele Identifier: CA360484966

Gene: CAST ERAP1

Linked Data

• MyVariant Identifiers: chr5:g.96098029A>G (hg19) ; chr5:g.96762325A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.96762325A>G , CM000667.2:g.96762325A>G	GRCh38
NC_000005.9:g.96098029A>G , CM000667.1:g.96098029A>G	GRCh37
NC_000005.8:g.96123785A>G	NCBI36
NG_027839.1:g.56820T>C
NG_029490.1:g.105289A>G
NG_027839.2:g.178659T>C
NG_029490.2:g.105289A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000484552.6:c.805A>G (CAST)	ENSP00000432878.2:p.Thr269Ala
ENST00000508608.6:c.1735A>G (CAST)	ENSP00000422677.2:p.Thr579Ala
ENST00000510756.6:c.1513A>G (CAST)	ENSP00000422176.2:p.Thr505Ala
ENST00000674587.1:c.1342A>G (CAST)	ENSP00000501797.1:p.Thr448Ala
ENST00000674702.1:c.1627A>G (CAST)	ENSP00000502345.1:p.Thr543Ala
ENST00000674984.1:c.1819A>G (CAST)	ENSP00000501713.1:p.Thr607Ala
ENST00000675033.1:c.1513A>G (CAST)	ENSP00000501659.1:p.Thr505Ala
ENST00000675179.1:c.1885A>G (CAST) MANE Select	ENSP00000501872.1:p.Thr629Ala
ENST00000675185.1:c.266A>G (CAST)
ENST00000675266.1:c.1787A>G (CAST)
ENST00000675267.1:c.*1509A>G (CAST)	ENSP00000502095.1:n.*1509A>G
ENST00000675275.1:c.602A>G (CAST)
ENST00000675479.1:c.1498A>G (CAST)	ENSP00000502244.1:p.Thr500Ala
ENST00000675614.1:c.1555A>G (CAST)	ENSP00000502136.1:p.Thr519Ala
ENST00000675663.1:c.1774A>G (CAST)	ENSP00000502449.1:p.Thr592Ala
ENST00000675734.1:n.429A>G (CAST)
ENST00000675858.1:c.1429A>G (CAST)	ENSP00000501780.1:p.Thr477Ala
ENST00000296754.7:c.*875T>C (ERAP1)	ENSP00000296754.3:n.*875T>C
ENST00000309190.9:c.1570A>G (CAST)	ENSP00000312523.5:p.Thr524Ala
ENST00000325674.11:c.805A>G (CAST)	ENSP00000320319.8:p.Thr269Ala
ENST00000338252.7:c.1597A>G (CAST)	ENSP00000343421.3:p.Thr533Ala
ENST00000341926.7:c.1636A>G (CAST)	ENSP00000339914.3:p.Thr546Ala
ENST00000348386.7:n.1578A>G (CAST)
ENST00000395812.6:c.1762A>G (CAST)	ENSP00000379157.2:p.Thr588Ala
ENST00000395813.5:c.1636A>G (CAST)	ENSP00000379158.2:p.Thr546Ala
ENST00000437034.6:c.891A>G (CAST)
ENST00000484552.5:c.863A>G (CAST)
ENST00000504465.5:c.1420A>G (CAST)	ENSP00000425670.1:p.Thr474Ala
ENST00000508579.5:c.781A>G (CAST)	ENSP00000425787.1:p.Thr261Ala
ENST00000508608.5:c.1774A>G (CAST)	ENSP00000422677.1:p.Thr592Ala
ENST00000508830.5:c.1885A>G (CAST)	ENSP00000425721.1:p.Thr629Ala
ENST00000509903.5:c.1531A>G (CAST)	ENSP00000426946.1:p.Thr511Ala
ENST00000510098.1:c.121A>G (CAST)	ENSP00000427195.1:p.Thr41Ala
ENST00000510156.5:c.1636A>G (CAST)	ENSP00000422325.1:p.Thr546Ala
ENST00000510500.5:c.908A>G (CAST)
ENST00000510756.5:c.1819A>G (CAST)	ENSP00000422176.1:p.Thr607Ala
ENST00000511049.5:c.1594A>G (CAST)	ENSP00000421130.1:p.Thr532Ala
ENST00000511782.5:c.1594A>G (CAST)	ENSP00000423638.1:p.Thr532Ala
ENST00000515663.5:c.805A>G (CAST)	ENSP00000422929.1:p.Thr269Ala
NM_001042440.3:c.1762A>G (CAST)	NP_001035905.1:p.Thr588Ala
NM_001190442.1:c.1597A>G (CAST)	NP_001177371.1:p.Thr533Ala
NM_001284212.1:c.1513A>G (CAST)	NP_001271141.1:p.Thr505Ala
NM_001284213.1:c.1420A>G (CAST)	NP_001271142.1:p.Thr474Ala
NM_016442.3:c.*875T>C (ERAP1)	NP_057526.3:n.*875T>C
NM_173060.3:c.1570A>G (CAST)	NP_775083.1:p.Thr524Ala
NR_104285.1:n.892A>G (CAST)
XM_006714696.2:c.1885A>G (CAST)	XP_006714759.1:p.Thr629Ala
XM_006714697.2:c.1885A>G (CAST)	XP_006714760.1:p.Thr629Ala
XM_006714698.2:c.1846A>G (CAST)	XP_006714761.1:p.Thr616Ala
XM_006714699.2:c.1840A>G (CAST)	XP_006714762.1:p.Thr614Ala
XM_006714700.2:c.1828A>G (CAST)	XP_006714763.1:p.Thr610Ala
XM_006714701.2:c.1819A>G (CAST)	XP_006714764.1:p.Thr607Ala
XM_006714702.2:c.1783A>G (CAST)	XP_006714765.1:p.Thr595Ala
XM_006714703.2:c.1780A>G (CAST)	XP_006714766.1:p.Thr594Ala
XM_006714704.2:c.1774A>G (CAST)	XP_006714767.1:p.Thr592Ala
XM_006714705.2:c.1762A>G (CAST)	XP_006714768.1:p.Thr588Ala
XM_006714706.2:c.1717A>G (CAST)	XP_006714769.1:p.Thr573Ala
XM_006714707.2:c.1636A>G (CAST)	XP_006714770.1:p.Thr546Ala
XM_006714708.2:c.1597A>G (CAST)	XP_006714771.1:p.Thr533Ala
XM_006714709.2:c.1579A>G (CAST)	XP_006714772.1:p.Thr527Ala
XM_006714710.2:c.1531A>G (CAST)	XP_006714773.1:p.Thr511Ala
XM_006714711.2:c.1513A>G (CAST)	XP_006714774.1:p.Thr505Ala
XM_006714712.2:c.1474A>G (CAST)	XP_006714775.1:p.Thr492Ala
XM_006714713.2:c.805A>G (CAST)	XP_006714776.1:p.Thr269Ala
XM_006714714.2:c.805A>G (CAST)	XP_006714777.1:p.Thr269Ala
XM_006714715.2:c.781A>G (CAST)	XP_006714778.1:p.Thr261Ala
XM_011543487.1:c.*875T>C (ERAP1)	XP_011541789.1:n.*875T>C
XM_011543654.1:c.1804A>G (CAST)	XP_011541956.1:p.Thr602Ala
XM_011543655.1:c.1801A>G (CAST)	XP_011541957.1:p.Thr601Ala
XM_011543656.1:c.1738A>G (CAST)	XP_011541958.1:p.Thr580Ala
XM_011543657.1:c.1693A>G (CAST)	XP_011541959.1:p.Thr565Ala
XM_011543658.1:c.1489A>G (CAST)	XP_011541960.1:p.Thr497Ala
NM_001042440.4:c.1762A>G (CAST)	NP_001035905.1:p.Thr588Ala
NM_001042441.2:c.1828A>G (CAST)	NP_001035906.1:p.Thr610Ala
NM_001042442.2:c.1819A>G (CAST)	NP_001035907.1:p.Thr607Ala
NM_001042443.2:c.1636A>G (CAST)	NP_001035908.1:p.Thr546Ala
NM_001042444.2:c.1513A>G (CAST)	NP_001035909.1:p.Thr505Ala
NM_001042445.2:c.1531A>G (CAST)	NP_001035910.1:p.Thr511Ala
NM_001042446.2:c.1474A>G (CAST)	NP_001035911.1:p.Thr492Ala
NM_001284212.3:c.1513A>G (CAST)	NP_001271141.1:p.Thr505Ala
NM_001284213.3:c.1420A>G (CAST)	NP_001271142.1:p.Thr474Ala
NM_001330626.1:c.1789A>G (CAST)	NP_001317555.1:p.Thr597Ala
NM_001330627.1:c.1762A>G (CAST)	NP_001317556.1:p.Thr588Ala
NM_001330628.1:c.1717A>G (CAST)	NP_001317557.1:p.Thr573Ala
NM_001330629.1:c.1801A>G (CAST)	NP_001317558.1:p.Thr601Ala
NM_001330630.1:c.1474A>G (CAST)	NP_001317559.1:p.Thr492Ala
NM_001330631.1:c.1597A>G (CAST)	NP_001317560.1:p.Thr533Ala
NM_001330632.1:c.1570A>G (CAST)	NP_001317561.1:p.Thr524Ala
NM_001330633.1:c.1579A>G (CAST)	NP_001317562.1:p.Thr527Ala
NM_001330634.1:c.1540A>G (CAST)	NP_001317563.1:p.Thr514Ala
NM_001349244.1:c.*875T>C (ERAP1)	NP_001336173.1:n.*875T>C
NM_001750.6:c.1885A>G (CAST)	NP_001741.4:p.Thr629Ala
NM_016442.4:c.*875T>C (ERAP1)	NP_057526.3:n.*875T>C
NM_173060.4:c.1570A>G (CAST)	NP_775083.1:p.Thr524Ala
XR_001742119.2:n.3860T>C (ERAP1)
NM_001042440.5:c.1762A>G (CAST)	NP_001035905.1:p.Thr588Ala
NM_001042441.3:c.1828A>G (CAST)	NP_001035906.1:p.Thr610Ala
NM_001042442.3:c.1819A>G (CAST)	NP_001035907.1:p.Thr607Ala
NM_001330626.2:c.1789A>G (CAST)	NP_001317555.1:p.Thr597Ala
NM_001330627.2:c.1762A>G (CAST)	NP_001317556.1:p.Thr588Ala
NM_001330628.2:c.1717A>G (CAST)	NP_001317557.1:p.Thr573Ala
NM_001330629.2:c.1801A>G (CAST)	NP_001317558.1:p.Thr601Ala
NM_001375317.1:c.1774A>G (CAST)	NP_001362246.1:p.Thr592Ala
NM_001750.7:c.1885A>G (CAST) MANE Select	NP_001741.4:p.Thr629Ala
NR_104285.2:n.830A>G (CAST)
NM_001042443.3:c.1636A>G (CAST)	NP_001035908.1:p.Thr546Ala
NM_001042444.3:c.1513A>G (CAST)	NP_001035909.1:p.Thr505Ala
NM_001042445.3:c.1531A>G (CAST)	NP_001035910.1:p.Thr511Ala
NM_001042446.3:c.1474A>G (CAST)	NP_001035911.1:p.Thr492Ala
NM_001190442.2:c.1597A>G (CAST)	NP_001177371.1:p.Thr533Ala
NM_001284212.4:c.1513A>G (CAST)	NP_001271141.1:p.Thr505Ala
NM_001284213.4:c.1420A>G (CAST)	NP_001271142.1:p.Thr474Ala
NM_001330630.2:c.1474A>G (CAST)	NP_001317559.1:p.Thr492Ala
NM_001330631.2:c.1597A>G (CAST)	NP_001317560.1:p.Thr533Ala
NM_001330632.2:c.1570A>G (CAST)	NP_001317561.1:p.Thr524Ala
NM_001330633.2:c.1579A>G (CAST)	NP_001317562.1:p.Thr527Ala
NM_001330634.2:c.1540A>G (CAST)	NP_001317563.1:p.Thr514Ala
NM_001349244.2:c.*875T>C (ERAP1)	NP_001336173.1:n.*875T>C
NM_016442.5:c.*875T>C (ERAP1)	NP_057526.3:n.*875T>C
NM_173060.5:c.1570A>G (CAST)	NP_775083.1:p.Thr524Ala