Canonical Allele Identifier: CA347591631

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874616A>C (hg19) ; chr2:g.88575098A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575098A>C , CM000664.2:g.88575098A>C	GRCh38
NC_000002.11:g.88874616A>C , CM000664.1:g.88874616A>C	GRCh37
NC_000002.10:g.88655731A>C	NCBI36
NG_016424.1:g.57479T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2213T>G
ENST00000682276.1:n.1830T>G
ENST00000682892.1:c.1932T>G	ENSP00000507214.1:p.Tyr644Ter
ENST00000682952.1:n.2024T>G
ENST00000684455.1:c.1598T>G
ENST00000684642.1:c.1782T>G	ENSP00000507355.1:p.Tyr594Ter
ENST00000684740.1:n.2563T>G
ENST00000303236.9:c.2385T>G MANE Select	ENSP00000307235.3:p.Tyr795Ter
ENST00000652099.1:c.2579T>G
ENST00000652736.1:n.2261T>G
ENST00000303236.7:c.2385T>G	ENSP00000307235.3:p.Tyr795Ter
ENST00000415570.1:c.2022T>G	ENSP00000412076.1:p.Tyr674Ter
ENST00000419748.5:c.1932T>G	ENSP00000408325.1:p.Tyr644Ter
ENST00000470706.1:n.49-21T>G
NM_001313915.1:c.1932T>G	NP_001300844.1:p.Tyr644Ter
NM_004836.5:c.2385T>G	NP_004827.4:p.Tyr795Ter
NM_004836.6:c.2385T>G	NP_004827.4:p.Tyr795Ter
NR_110236.1:n.1235A>C
XM_005264649.3:c.1701T>G	XP_005264706.1:p.Tyr567Ter
XM_017005376.2:c.1701T>G	XP_016860865.1:p.Tyr567Ter
NM_004836.7:c.2385T>G MANE Select	NP_004827.4:p.Tyr795Ter
NM_001313915.2:c.1932T>G	NP_001300844.1:p.Tyr644Ter