Canonical Allele Identifier: CA347592994

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874938C>T (hg19) ; chr2:g.88575420C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575420C>T , CM000664.2:g.88575420C>T	GRCh38
NC_000002.11:g.88874938C>T , CM000664.1:g.88874938C>T	GRCh37
NC_000002.10:g.88656053C>T	NCBI36
NG_016424.1:g.57157G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.1891G>A
ENST00000682276.1:n.1508G>A
ENST00000682892.1:c.1610G>A	ENSP00000507214.1:p.Ser537Asn
ENST00000682952.1:n.1702G>A
ENST00000684455.1:c.1276G>A
ENST00000684642.1:c.1460G>A	ENSP00000507355.1:p.Ser487Asn
ENST00000684740.1:n.2241G>A
ENST00000303236.9:c.2063G>A MANE Select	ENSP00000307235.3:p.Ser688Asn
ENST00000652099.1:c.2257G>A
ENST00000652736.1:n.1939G>A
ENST00000303236.7:c.2063G>A	ENSP00000307235.3:p.Ser688Asn
ENST00000415570.1:c.1700G>A	ENSP00000412076.1:p.Ser567Asn
ENST00000419748.5:c.1610G>A	ENSP00000408325.1:p.Ser537Asn
ENST00000478003.1:n.629G>A
NM_001313915.1:c.1610G>A	NP_001300844.1:p.Ser537Asn
NM_004836.5:c.2063G>A	NP_004827.4:p.Ser688Asn
NM_004836.6:c.2063G>A	NP_004827.4:p.Ser688Asn
NR_110236.1:n.1557C>T
XM_005264649.3:c.1379G>A	XP_005264706.1:p.Ser460Asn
XR_939749.1:n.2342G>A
XM_017005376.2:c.1379G>A	XP_016860865.1:p.Ser460Asn
NM_004836.7:c.2063G>A MANE Select	NP_004827.4:p.Ser688Asn
NM_001313915.2:c.1610G>A	NP_001300844.1:p.Ser537Asn