Canonical Allele Identifier: CA347593938

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88882946A>C (hg19) ; chr2:g.88583428A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88583428A>C , CM000664.2:g.88583428A>C	GRCh38
NC_000002.11:g.88882946A>C , CM000664.1:g.88882946A>C	GRCh37
NC_000002.10:g.88664061A>C	NCBI36
NG_016424.1:g.49149T>G

Transcript Alleles

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