Canonical Allele Identifier: CA347592997

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874939T>G (hg19) ; chr2:g.88575421T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575421T>G , CM000664.2:g.88575421T>G	GRCh38
NC_000002.11:g.88874939T>G , CM000664.1:g.88874939T>G	GRCh37
NC_000002.10:g.88656054T>G	NCBI36
NG_016424.1:g.57156A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.1890A>C
ENST00000682276.1:n.1507A>C
ENST00000682892.1:c.1609A>C	ENSP00000507214.1:p.Ser537Arg
ENST00000682952.1:n.1701A>C
ENST00000684455.1:c.1275A>C
ENST00000684642.1:c.1459A>C	ENSP00000507355.1:p.Ser487Arg
ENST00000684740.1:n.2240A>C
ENST00000303236.9:c.2062A>C MANE Select	ENSP00000307235.3:p.Ser688Arg
ENST00000652099.1:c.2256A>C
ENST00000652736.1:n.1938A>C
ENST00000303236.7:c.2062A>C	ENSP00000307235.3:p.Ser688Arg
ENST00000415570.1:c.1699A>C	ENSP00000412076.1:p.Ser567Arg
ENST00000419748.5:c.1609A>C	ENSP00000408325.1:p.Ser537Arg
ENST00000478003.1:n.628A>C
NM_001313915.1:c.1609A>C	NP_001300844.1:p.Ser537Arg
NM_004836.5:c.2062A>C	NP_004827.4:p.Ser688Arg
NM_004836.6:c.2062A>C	NP_004827.4:p.Ser688Arg
NR_110236.1:n.1558T>G
XM_005264649.3:c.1378A>C	XP_005264706.1:p.Ser460Arg
XR_939749.1:n.2341A>C
XM_017005376.2:c.1378A>C	XP_016860865.1:p.Ser460Arg
NM_004836.7:c.2062A>C MANE Select	NP_004827.4:p.Ser688Arg
NM_001313915.2:c.1609A>C	NP_001300844.1:p.Ser537Arg