Canonical Allele Identifier: CA427445344

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874733A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575215A>G , CM000664.2:g.88575215A>G	GRCh38
NC_000002.11:g.88874733A>G , CM000664.1:g.88874733A>G	GRCh37
NC_000002.10:g.88655848A>G	NCBI36
NG_016424.1:g.57362T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2096T>C
ENST00000682276.1:n.1713T>C
ENST00000682892.1:c.1815T>C	ENSP00000507214.1:p.Asp605=
ENST00000682952.1:n.1907T>C
ENST00000684455.1:c.1481T>C
ENST00000684642.1:c.1665T>C	ENSP00000507355.1:p.Asp555=
ENST00000684740.1:n.2446T>C
ENST00000303236.9:c.2268T>C MANE Select	ENSP00000307235.3:p.Asp756=
ENST00000652099.1:c.2462T>C
ENST00000652736.1:n.2144T>C
ENST00000303236.7:c.2268T>C	ENSP00000307235.3:p.Asp756=
ENST00000415570.1:c.1905T>C	ENSP00000412076.1:p.Asp635=
ENST00000419748.5:c.1815T>C	ENSP00000408325.1:p.Asp605=
ENST00000470706.1:n.49-138T>C
NM_001313915.1:c.1815T>C	NP_001300844.1:p.Asp605=
NM_004836.5:c.2268T>C	NP_004827.4:p.Asp756=
NM_004836.6:c.2268T>C	NP_004827.4:p.Asp756=
NR_110236.1:n.1352A>G
XM_005264649.3:c.1584T>C	XP_005264706.1:p.Asp528=
XM_017005376.2:c.1584T>C	XP_016860865.1:p.Asp528=
NM_004836.7:c.2268T>C MANE Select	NP_004827.4:p.Asp756=
NM_001313915.2:c.1815T>C	NP_001300844.1:p.Asp605=