Canonical Allele Identifier: CA360485006

Gene: CAST ERAP1

Linked Data

• MyVariant Identifiers: chr5:g.96098050G>A (hg19) ; chr5:g.96762346G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.96762346G>A , CM000667.2:g.96762346G>A	GRCh38
NC_000005.9:g.96098050G>A , CM000667.1:g.96098050G>A	GRCh37
NC_000005.8:g.96123806G>A	NCBI36
NG_027839.1:g.56799C>T
NG_029490.1:g.105310G>A
NG_027839.2:g.178638C>T
NG_029490.2:g.105310G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000484552.6:c.826G>A (CAST)	ENSP00000432878.2:p.Ala276Thr
ENST00000508608.6:c.1756G>A (CAST)	ENSP00000422677.2:p.Ala586Thr
ENST00000510756.6:c.1534G>A (CAST)	ENSP00000422176.2:p.Ala512Thr
ENST00000674587.1:c.1363G>A (CAST)	ENSP00000501797.1:p.Ala455Thr
ENST00000674702.1:c.1648G>A (CAST)	ENSP00000502345.1:p.Ala550Thr
ENST00000674984.1:c.1840G>A (CAST)	ENSP00000501713.1:p.Ala614Thr
ENST00000675033.1:c.1534G>A (CAST)	ENSP00000501659.1:p.Ala512Thr
ENST00000675179.1:c.1906G>A (CAST) MANE Select	ENSP00000501872.1:p.Ala636Thr
ENST00000675185.1:c.287G>A (CAST)
ENST00000675266.1:c.1808G>A (CAST)
ENST00000675267.1:c.*1530G>A (CAST)	ENSP00000502095.1:n.*1530G>A
ENST00000675275.1:c.623G>A (CAST)
ENST00000675479.1:c.1519G>A (CAST)	ENSP00000502244.1:p.Ala507Thr
ENST00000675614.1:c.1576G>A (CAST)	ENSP00000502136.1:p.Ala526Thr
ENST00000675663.1:c.1795G>A (CAST)	ENSP00000502449.1:p.Ala599Thr
ENST00000675734.1:n.450G>A (CAST)
ENST00000675858.1:c.1450G>A (CAST)	ENSP00000501780.1:p.Ala484Thr
ENST00000296754.7:c.*854C>T (ERAP1)	ENSP00000296754.3:n.*854C>T
ENST00000309190.9:c.1591G>A (CAST)	ENSP00000312523.5:p.Ala531Thr
ENST00000325674.11:c.826G>A (CAST)	ENSP00000320319.8:p.Ala276Thr
ENST00000338252.7:c.1618G>A (CAST)	ENSP00000343421.3:p.Ala540Thr
ENST00000341926.7:c.1657G>A (CAST)	ENSP00000339914.3:p.Ala553Thr
ENST00000348386.7:n.1599G>A (CAST)
ENST00000395812.6:c.1783G>A (CAST)	ENSP00000379157.2:p.Ala595Thr
ENST00000395813.5:c.1657G>A (CAST)	ENSP00000379158.2:p.Ala553Thr
ENST00000437034.6:c.912G>A (CAST)
ENST00000484552.5:c.884G>A (CAST)
ENST00000504465.5:c.1441G>A (CAST)	ENSP00000425670.1:p.Ala481Thr
ENST00000508579.5:c.802G>A (CAST)	ENSP00000425787.1:p.Ala268Thr
ENST00000508608.5:c.1795G>A (CAST)	ENSP00000422677.1:p.Ala599Thr
ENST00000508830.5:c.1906G>A (CAST)	ENSP00000425721.1:p.Ala636Thr
ENST00000509903.5:c.1552G>A (CAST)	ENSP00000426946.1:p.Ala518Thr
ENST00000510098.1:c.142G>A (CAST)	ENSP00000427195.1:p.Ala48Thr
ENST00000510156.5:c.1657G>A (CAST)	ENSP00000422325.1:p.Ala553Thr
ENST00000510500.5:c.929G>A (CAST)
ENST00000510756.5:c.1840G>A (CAST)	ENSP00000422176.1:p.Ala614Thr
ENST00000511049.5:c.1615G>A (CAST)	ENSP00000421130.1:p.Ala539Thr
ENST00000511782.5:c.1615G>A (CAST)	ENSP00000423638.1:p.Ala539Thr
ENST00000515663.5:c.826G>A (CAST)	ENSP00000422929.1:p.Ala276Thr
NM_001042440.3:c.1783G>A (CAST)	NP_001035905.1:p.Ala595Thr
NM_001190442.1:c.1618G>A (CAST)	NP_001177371.1:p.Ala540Thr
NM_001284212.1:c.1534G>A (CAST)	NP_001271141.1:p.Ala512Thr
NM_001284213.1:c.1441G>A (CAST)	NP_001271142.1:p.Ala481Thr
NM_016442.3:c.*854C>T (ERAP1)	NP_057526.3:n.*854C>T
NM_173060.3:c.1591G>A (CAST)	NP_775083.1:p.Ala531Thr
NR_104285.1:n.913G>A (CAST)
XM_006714696.2:c.1906G>A (CAST)	XP_006714759.1:p.Ala636Thr
XM_006714697.2:c.1906G>A (CAST)	XP_006714760.1:p.Ala636Thr
XM_006714698.2:c.1867G>A (CAST)	XP_006714761.1:p.Ala623Thr
XM_006714699.2:c.1861G>A (CAST)	XP_006714762.1:p.Ala621Thr
XM_006714700.2:c.1849G>A (CAST)	XP_006714763.1:p.Ala617Thr
XM_006714701.2:c.1840G>A (CAST)	XP_006714764.1:p.Ala614Thr
XM_006714702.2:c.1804G>A (CAST)	XP_006714765.1:p.Ala602Thr
XM_006714703.2:c.1801G>A (CAST)	XP_006714766.1:p.Ala601Thr
XM_006714704.2:c.1795G>A (CAST)	XP_006714767.1:p.Ala599Thr
XM_006714705.2:c.1783G>A (CAST)	XP_006714768.1:p.Ala595Thr
XM_006714706.2:c.1738G>A (CAST)	XP_006714769.1:p.Ala580Thr
XM_006714707.2:c.1657G>A (CAST)	XP_006714770.1:p.Ala553Thr
XM_006714708.2:c.1618G>A (CAST)	XP_006714771.1:p.Ala540Thr
XM_006714709.2:c.1600G>A (CAST)	XP_006714772.1:p.Ala534Thr
XM_006714710.2:c.1552G>A (CAST)	XP_006714773.1:p.Ala518Thr
XM_006714711.2:c.1534G>A (CAST)	XP_006714774.1:p.Ala512Thr
XM_006714712.2:c.1495G>A (CAST)	XP_006714775.1:p.Ala499Thr
XM_006714713.2:c.826G>A (CAST)	XP_006714776.1:p.Ala276Thr
XM_006714714.2:c.826G>A (CAST)	XP_006714777.1:p.Ala276Thr
XM_006714715.2:c.802G>A (CAST)	XP_006714778.1:p.Ala268Thr
XM_011543487.1:c.*854C>T (ERAP1)	XP_011541789.1:n.*854C>T
XM_011543654.1:c.1825G>A (CAST)	XP_011541956.1:p.Ala609Thr
XM_011543655.1:c.1822G>A (CAST)	XP_011541957.1:p.Ala608Thr
XM_011543656.1:c.1759G>A (CAST)	XP_011541958.1:p.Ala587Thr
XM_011543657.1:c.1714G>A (CAST)	XP_011541959.1:p.Ala572Thr
XM_011543658.1:c.1510G>A (CAST)	XP_011541960.1:p.Ala504Thr
NM_001042440.4:c.1783G>A (CAST)	NP_001035905.1:p.Ala595Thr
NM_001042441.2:c.1849G>A (CAST)	NP_001035906.1:p.Ala617Thr
NM_001042442.2:c.1840G>A (CAST)	NP_001035907.1:p.Ala614Thr
NM_001042443.2:c.1657G>A (CAST)	NP_001035908.1:p.Ala553Thr
NM_001042444.2:c.1534G>A (CAST)	NP_001035909.1:p.Ala512Thr
NM_001042445.2:c.1552G>A (CAST)	NP_001035910.1:p.Ala518Thr
NM_001042446.2:c.1495G>A (CAST)	NP_001035911.1:p.Ala499Thr
NM_001284212.3:c.1534G>A (CAST)	NP_001271141.1:p.Ala512Thr
NM_001284213.3:c.1441G>A (CAST)	NP_001271142.1:p.Ala481Thr
NM_001330626.1:c.1810G>A (CAST)	NP_001317555.1:p.Ala604Thr
NM_001330627.1:c.1783G>A (CAST)	NP_001317556.1:p.Ala595Thr
NM_001330628.1:c.1738G>A (CAST)	NP_001317557.1:p.Ala580Thr
NM_001330629.1:c.1822G>A (CAST)	NP_001317558.1:p.Ala608Thr
NM_001330630.1:c.1495G>A (CAST)	NP_001317559.1:p.Ala499Thr
NM_001330631.1:c.1618G>A (CAST)	NP_001317560.1:p.Ala540Thr
NM_001330632.1:c.1591G>A (CAST)	NP_001317561.1:p.Ala531Thr
NM_001330633.1:c.1600G>A (CAST)	NP_001317562.1:p.Ala534Thr
NM_001330634.1:c.1561G>A (CAST)	NP_001317563.1:p.Ala521Thr
NM_001349244.1:c.*854C>T (ERAP1)	NP_001336173.1:n.*854C>T
NM_001750.6:c.1906G>A (CAST)	NP_001741.4:p.Ala636Thr
NM_016442.4:c.*854C>T (ERAP1)	NP_057526.3:n.*854C>T
NM_173060.4:c.1591G>A (CAST)	NP_775083.1:p.Ala531Thr
XR_001742119.2:n.3839C>T (ERAP1)
NM_001042440.5:c.1783G>A (CAST)	NP_001035905.1:p.Ala595Thr
NM_001042441.3:c.1849G>A (CAST)	NP_001035906.1:p.Ala617Thr
NM_001042442.3:c.1840G>A (CAST)	NP_001035907.1:p.Ala614Thr
NM_001330626.2:c.1810G>A (CAST)	NP_001317555.1:p.Ala604Thr
NM_001330627.2:c.1783G>A (CAST)	NP_001317556.1:p.Ala595Thr
NM_001330628.2:c.1738G>A (CAST)	NP_001317557.1:p.Ala580Thr
NM_001330629.2:c.1822G>A (CAST)	NP_001317558.1:p.Ala608Thr
NM_001375317.1:c.1795G>A (CAST)	NP_001362246.1:p.Ala599Thr
NM_001750.7:c.1906G>A (CAST) MANE Select	NP_001741.4:p.Ala636Thr
NR_104285.2:n.851G>A (CAST)
NM_001042443.3:c.1657G>A (CAST)	NP_001035908.1:p.Ala553Thr
NM_001042444.3:c.1534G>A (CAST)	NP_001035909.1:p.Ala512Thr
NM_001042445.3:c.1552G>A (CAST)	NP_001035910.1:p.Ala518Thr
NM_001042446.3:c.1495G>A (CAST)	NP_001035911.1:p.Ala499Thr
NM_001190442.2:c.1618G>A (CAST)	NP_001177371.1:p.Ala540Thr
NM_001284212.4:c.1534G>A (CAST)	NP_001271141.1:p.Ala512Thr
NM_001284213.4:c.1441G>A (CAST)	NP_001271142.1:p.Ala481Thr
NM_001330630.2:c.1495G>A (CAST)	NP_001317559.1:p.Ala499Thr
NM_001330631.2:c.1618G>A (CAST)	NP_001317560.1:p.Ala540Thr
NM_001330632.2:c.1591G>A (CAST)	NP_001317561.1:p.Ala531Thr
NM_001330633.2:c.1600G>A (CAST)	NP_001317562.1:p.Ala534Thr
NM_001330634.2:c.1561G>A (CAST)	NP_001317563.1:p.Ala521Thr
NM_001349244.2:c.*854C>T (ERAP1)	NP_001336173.1:n.*854C>T
NM_016442.5:c.*854C>T (ERAP1)	NP_057526.3:n.*854C>T
NM_173060.5:c.1591G>A (CAST)	NP_775083.1:p.Ala531Thr