Canonical Allele Identifier: CA427173221

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874925T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575407T>G , CM000664.2:g.88575407T>G	GRCh38
NC_000002.11:g.88874925T>G , CM000664.1:g.88874925T>G	GRCh37
NC_000002.10:g.88656040T>G	NCBI36
NG_016424.1:g.57170A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.1904A>C
ENST00000682276.1:n.1521A>C
ENST00000682892.1:c.1623A>C	ENSP00000507214.1:p.Ala541=
ENST00000682952.1:n.1715A>C
ENST00000684455.1:c.1289A>C
ENST00000684642.1:c.1473A>C	ENSP00000507355.1:p.Ala491=
ENST00000684740.1:n.2254A>C
ENST00000303236.9:c.2076A>C MANE Select	ENSP00000307235.3:p.Ala692=
ENST00000652099.1:c.2270A>C
ENST00000652736.1:n.1952A>C
ENST00000303236.7:c.2076A>C	ENSP00000307235.3:p.Ala692=
ENST00000415570.1:c.1713A>C	ENSP00000412076.1:p.Ala571=
ENST00000419748.5:c.1623A>C	ENSP00000408325.1:p.Ala541=
ENST00000470706.1:n.2A>C
ENST00000478003.1:n.642A>C
NM_001313915.1:c.1623A>C	NP_001300844.1:p.Ala541=
NM_004836.5:c.2076A>C	NP_004827.4:p.Ala692=
NM_004836.6:c.2076A>C	NP_004827.4:p.Ala692=
NR_110236.1:n.1544T>G
XM_005264649.3:c.1392A>C	XP_005264706.1:p.Ala464=
XR_939749.1:n.2355A>C
XM_017005376.2:c.1392A>C	XP_016860865.1:p.Ala464=
NM_004836.7:c.2076A>C MANE Select	NP_004827.4:p.Ala692=
NM_001313915.2:c.1623A>C	NP_001300844.1:p.Ala541=