Canonical Allele Identifier: CA51491895

Gene: EIF2AK3

Linked Data

• dbSNP Id: rs934212885
• gnomAD v4: 2-88583383-G-A
• MyVariant Identifiers: chr2:g.88882901G>A (hg19) ; chr2:g.88583383G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88583383G>A , CM000664.2:g.88583383G>A	GRCh38
NC_000002.11:g.88882901G>A , CM000664.1:g.88882901G>A	GRCh37
NC_000002.10:g.88664016G>A	NCBI36
NG_016424.1:g.49194C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682276.1:n.1208+47C>T
ENST00000682892.1:c.1310+47C>T	ENSP00000507214.1:n.1310+47C>T
ENST00000682952.1:n.1402+47C>T
ENST00000684455.1:c.976+47C>T
ENST00000684642.1:c.1160+47C>T	ENSP00000507355.1:n.1160+47C>T
ENST00000303236.9:c.1763+47C>T MANE Select	ENSP00000307235.3:n.1763+47C>T
ENST00000652099.1:c.1957+47C>T
ENST00000652736.1:n.1639+47C>T
ENST00000303236.7:c.1763+47C>T	ENSP00000307235.3:n.1763+47C>T
ENST00000415570.1:c.1400+47C>T	ENSP00000412076.1:n.1400+47C>T
ENST00000419748.5:c.1310+47C>T	ENSP00000408325.1:n.1310+47C>T
NM_001313915.1:c.1310+47C>T	NP_001300844.1:n.1310+47C>T
NM_004836.5:c.1763+47C>T	NP_004827.4:n.1763+47C>T
NM_004836.6:c.1763+47C>T	NP_004827.4:n.1763+47C>T
XM_005264649.3:c.1079+47C>T	XP_005264706.1:n.1079+47C>T
XR_939749.1:n.1972+47C>T
XM_017005376.2:c.1079+47C>T	XP_016860865.1:n.1079+47C>T
NM_004836.7:c.1763+47C>T MANE Select	NP_004827.4:n.1763+47C>T
NM_001313915.2:c.1310+47C>T	NP_001300844.1:n.1310+47C>T