Canonical Allele Identifier: CA347591396

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874563C>G (hg19) ; chr2:g.88575045C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575045C>G , CM000664.2:g.88575045C>G	GRCh38
NC_000002.11:g.88874563C>G , CM000664.1:g.88874563C>G	GRCh37
NC_000002.10:g.88655678C>G	NCBI36
NG_016424.1:g.57532G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2266G>C
ENST00000682276.1:n.1883G>C
ENST00000682892.1:c.1985G>C	ENSP00000507214.1:p.Cys662Ser
ENST00000682952.1:n.2077G>C
ENST00000684455.1:c.1651G>C
ENST00000684642.1:c.1835G>C	ENSP00000507355.1:p.Cys612Ser
ENST00000684740.1:n.2616G>C
ENST00000303236.9:c.2438G>C MANE Select	ENSP00000307235.3:p.Cys813Ser
ENST00000652099.1:c.2632G>C
ENST00000652736.1:n.2314G>C
ENST00000303236.7:c.2438G>C	ENSP00000307235.3:p.Cys813Ser
ENST00000415570.1:c.2075G>C	ENSP00000412076.1:p.Cys692Ser
ENST00000419748.5:c.1985G>C	ENSP00000408325.1:p.Cys662Ser
ENST00000470706.1:n.81G>C
NM_001313915.1:c.1985G>C	NP_001300844.1:p.Cys662Ser
NM_004836.5:c.2438G>C	NP_004827.4:p.Cys813Ser
NM_004836.6:c.2438G>C	NP_004827.4:p.Cys813Ser
NR_110236.1:n.1182C>G
XM_005264649.3:c.1754G>C	XP_005264706.1:p.Cys585Ser
XM_017005376.2:c.1754G>C	XP_016860865.1:p.Cys585Ser
NM_004836.7:c.2438G>C MANE Select	NP_004827.4:p.Cys813Ser
NM_001313915.2:c.1985G>C	NP_001300844.1:p.Cys662Ser