Canonical Allele Identifier: CA347591644

Gene: EIF2AK3

Linked Data

• gnomAD v4: 2-88575100-A-G
• MyVariant Identifiers: chr2:g.88874618A>G (hg19) ; chr2:g.88575100A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575100A>G , CM000664.2:g.88575100A>G	GRCh38
NC_000002.11:g.88874618A>G , CM000664.1:g.88874618A>G	GRCh37
NC_000002.10:g.88655733A>G	NCBI36
NG_016424.1:g.57477T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2211T>C
ENST00000682276.1:n.1828T>C
ENST00000682892.1:c.1930T>C	ENSP00000507214.1:p.Tyr644His
ENST00000682952.1:n.2022T>C
ENST00000684455.1:c.1596T>C
ENST00000684642.1:c.1780T>C	ENSP00000507355.1:p.Tyr594His
ENST00000684740.1:n.2561T>C
ENST00000303236.9:c.2383T>C MANE Select	ENSP00000307235.3:p.Tyr795His
ENST00000652099.1:c.2577T>C
ENST00000652736.1:n.2259T>C
ENST00000303236.7:c.2383T>C	ENSP00000307235.3:p.Tyr795His
ENST00000415570.1:c.2020T>C	ENSP00000412076.1:p.Tyr674His
ENST00000419748.5:c.1930T>C	ENSP00000408325.1:p.Tyr644His
ENST00000470706.1:n.49-23T>C
NM_001313915.1:c.1930T>C	NP_001300844.1:p.Tyr644His
NM_004836.5:c.2383T>C	NP_004827.4:p.Tyr795His
NM_004836.6:c.2383T>C	NP_004827.4:p.Tyr795His
NR_110236.1:n.1237A>G
XM_005264649.3:c.1699T>C	XP_005264706.1:p.Tyr567His
XM_017005376.2:c.1699T>C	XP_016860865.1:p.Tyr567His
NM_004836.7:c.2383T>C MANE Select	NP_004827.4:p.Tyr795His
NM_001313915.2:c.1930T>C	NP_001300844.1:p.Tyr644His