Canonical Allele Identifier: CA347592334

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874768C>A (hg19) ; chr2:g.88575250C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575250C>A , CM000664.2:g.88575250C>A	GRCh38
NC_000002.11:g.88874768C>A , CM000664.1:g.88874768C>A	GRCh37
NC_000002.10:g.88655883C>A	NCBI36
NG_016424.1:g.57327G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2061G>T
ENST00000682276.1:n.1678G>T
ENST00000682892.1:c.1780G>T	ENSP00000507214.1:p.Gly594Ter
ENST00000682952.1:n.1872G>T
ENST00000684455.1:c.1446G>T
ENST00000684642.1:c.1630G>T	ENSP00000507355.1:p.Gly544Ter
ENST00000684740.1:n.2411G>T
ENST00000303236.9:c.2233G>T MANE Select	ENSP00000307235.3:p.Gly745Ter
ENST00000652099.1:c.2427G>T
ENST00000652736.1:n.2109G>T
ENST00000303236.7:c.2233G>T	ENSP00000307235.3:p.Gly745Ter
ENST00000415570.1:c.1870G>T	ENSP00000412076.1:p.Gly624Ter
ENST00000419748.5:c.1780G>T	ENSP00000408325.1:p.Gly594Ter
ENST00000470706.1:n.48+111G>T
NM_001313915.1:c.1780G>T	NP_001300844.1:p.Gly594Ter
NM_004836.5:c.2233G>T	NP_004827.4:p.Gly745Ter
NM_004836.6:c.2233G>T	NP_004827.4:p.Gly745Ter
NR_110236.1:n.1387C>A
XM_005264649.3:c.1549G>T	XP_005264706.1:p.Gly517Ter
XM_017005376.2:c.1549G>T	XP_016860865.1:p.Gly517Ter
NM_004836.7:c.2233G>T MANE Select	NP_004827.4:p.Gly745Ter
NM_001313915.2:c.1780G>T	NP_001300844.1:p.Gly594Ter