Canonical Allele Identifier: CA347593025

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874954G>C (hg19) ; chr2:g.88575436G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575436G>C , CM000664.2:g.88575436G>C	GRCh38
NC_000002.11:g.88874954G>C , CM000664.1:g.88874954G>C	GRCh37
NC_000002.10:g.88656069G>C	NCBI36
NG_016424.1:g.57141C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.1875C>G
ENST00000682276.1:n.1492C>G
ENST00000682892.1:c.1594C>G	ENSP00000507214.1:p.Pro532Ala
ENST00000682952.1:n.1686C>G
ENST00000684455.1:c.1260C>G
ENST00000684642.1:c.1444C>G	ENSP00000507355.1:p.Pro482Ala
ENST00000684740.1:n.2225C>G
ENST00000303236.9:c.2047C>G MANE Select	ENSP00000307235.3:p.Pro683Ala
ENST00000652099.1:c.2241C>G
ENST00000652736.1:n.1923C>G
ENST00000303236.7:c.2047C>G	ENSP00000307235.3:p.Pro683Ala
ENST00000415570.1:c.1684C>G	ENSP00000412076.1:p.Pro562Ala
ENST00000419748.5:c.1594C>G	ENSP00000408325.1:p.Pro532Ala
ENST00000478003.1:n.613C>G
NM_001313915.1:c.1594C>G	NP_001300844.1:p.Pro532Ala
NM_004836.5:c.2047C>G	NP_004827.4:p.Pro683Ala
NM_004836.6:c.2047C>G	NP_004827.4:p.Pro683Ala
NR_110236.1:n.1573G>C
XM_005264649.3:c.1363C>G	XP_005264706.1:p.Pro455Ala
XR_939749.1:n.2326C>G
XM_017005376.2:c.1363C>G	XP_016860865.1:p.Pro455Ala
NM_004836.7:c.2047C>G MANE Select	NP_004827.4:p.Pro683Ala
NM_001313915.2:c.1594C>G	NP_001300844.1:p.Pro532Ala