Canonical Allele Identifier: CA347591443

Gene: EIF2AK3

Linked Data

• gnomAD v4: 2-88575056-T-G
• MyVariant Identifiers: chr2:g.88874574T>G (hg19) ; chr2:g.88575056T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575056T>G , CM000664.2:g.88575056T>G	GRCh38
NC_000002.11:g.88874574T>G , CM000664.1:g.88874574T>G	GRCh37
NC_000002.10:g.88655689T>G	NCBI36
NG_016424.1:g.57521A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2255A>C
ENST00000682276.1:n.1872A>C
ENST00000682892.1:c.1974A>C	ENSP00000507214.1:p.Glu658Asp
ENST00000682952.1:n.2066A>C
ENST00000684455.1:c.1640A>C
ENST00000684642.1:c.1824A>C	ENSP00000507355.1:p.Glu608Asp
ENST00000684740.1:n.2605A>C
ENST00000303236.9:c.2427A>C MANE Select	ENSP00000307235.3:p.Glu809Asp
ENST00000652099.1:c.2621A>C
ENST00000652736.1:n.2303A>C
ENST00000303236.7:c.2427A>C	ENSP00000307235.3:p.Glu809Asp
ENST00000415570.1:c.2064A>C	ENSP00000412076.1:p.Glu688Asp
ENST00000419748.5:c.1974A>C	ENSP00000408325.1:p.Glu658Asp
ENST00000470706.1:n.70A>C
NM_001313915.1:c.1974A>C	NP_001300844.1:p.Glu658Asp
NM_004836.5:c.2427A>C	NP_004827.4:p.Glu809Asp
NM_004836.6:c.2427A>C	NP_004827.4:p.Glu809Asp
NR_110236.1:n.1193T>G
XM_005264649.3:c.1743A>C	XP_005264706.1:p.Glu581Asp
XM_017005376.2:c.1743A>C	XP_016860865.1:p.Glu581Asp
NM_004836.7:c.2427A>C MANE Select	NP_004827.4:p.Glu809Asp
NM_001313915.2:c.1974A>C	NP_001300844.1:p.Glu658Asp