Canonical Allele Identifier: CA347591236

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874528T>C (hg19) ; chr2:g.88575010T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575010T>C , CM000664.2:g.88575010T>C	GRCh38
NC_000002.11:g.88874528T>C , CM000664.1:g.88874528T>C	GRCh37
NC_000002.10:g.88655643T>C	NCBI36
NG_016424.1:g.57567A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2301A>G
ENST00000682103.1:c.14A>G
ENST00000682276.1:n.1918A>G
ENST00000682892.1:c.2020A>G	ENSP00000507214.1:p.Asn674Asp
ENST00000682952.1:n.2112A>G
ENST00000684455.1:c.1686A>G
ENST00000684642.1:c.1870A>G	ENSP00000507355.1:p.Asn624Asp
ENST00000684740.1:n.2651A>G
ENST00000303236.9:c.2473A>G MANE Select	ENSP00000307235.3:p.Asn825Asp
ENST00000652099.1:c.2667A>G
ENST00000652736.1:n.2349A>G
ENST00000303236.7:c.2473A>G	ENSP00000307235.3:p.Asn825Asp
ENST00000415570.1:c.2110A>G	ENSP00000412076.1:p.Asn704Asp
ENST00000419748.5:c.2020A>G	ENSP00000408325.1:p.Asn674Asp
ENST00000470706.1:n.116A>G
NM_001313915.1:c.2020A>G	NP_001300844.1:p.Asn674Asp
NM_004836.5:c.2473A>G	NP_004827.4:p.Asn825Asp
NM_004836.6:c.2473A>G	NP_004827.4:p.Asn825Asp
NR_110236.1:n.1147T>C
XM_005264649.3:c.1789A>G	XP_005264706.1:p.Asn597Asp
XM_017005376.2:c.1789A>G	XP_016860865.1:p.Asn597Asp
NM_004836.7:c.2473A>G MANE Select	NP_004827.4:p.Asn825Asp
NM_001313915.2:c.2020A>G	NP_001300844.1:p.Asn674Asp