Canonical Allele Identifier: CA347592993

Gene: EIF2AK3

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.1891G>C
ENST00000682276.1:n.1508G>C
ENST00000682892.1:c.1610G>C	ENSP00000507214.1:p.Ser537Thr
ENST00000682952.1:n.1702G>C
ENST00000684455.1:c.1276G>C
ENST00000684642.1:c.1460G>C	ENSP00000507355.1:p.Ser487Thr
ENST00000684740.1:n.2241G>C
ENST00000303236.9:c.2063G>C MANE Select	ENSP00000307235.3:p.Ser688Thr
ENST00000652099.1:c.2257G>C
ENST00000652736.1:n.1939G>C
ENST00000303236.7:c.2063G>C	ENSP00000307235.3:p.Ser688Thr
ENST00000415570.1:c.1700G>C	ENSP00000412076.1:p.Ser567Thr
ENST00000419748.5:c.1610G>C	ENSP00000408325.1:p.Ser537Thr
ENST00000478003.1:n.629G>C
NM_001313915.1:c.1610G>C	NP_001300844.1:p.Ser537Thr
NM_004836.5:c.2063G>C	NP_004827.4:p.Ser688Thr
NM_004836.6:c.2063G>C	NP_004827.4:p.Ser688Thr
NR_110236.1:n.1557C>G
XM_005264649.3:c.1379G>C	XP_005264706.1:p.Ser460Thr
XR_939749.1:n.2342G>C
XM_017005376.2:c.1379G>C	XP_016860865.1:p.Ser460Thr
NM_004836.7:c.2063G>C MANE Select	NP_004827.4:p.Ser688Thr
NM_001313915.2:c.1610G>C	NP_001300844.1:p.Ser537Thr