Canonical Allele Identifier: CA1268216897

Gene: EIF2AK3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88595833T= , CM000664.2:g.88595833T=	GRCh38
NC_000002.11:g.88895351T= , CM000664.1:g.88895351T=	GRCh37
NC_000002.10:g.88676466T=	NCBI36
NG_016424.1:g.36744A=

Transcript Alleles

HGVS	Amino-acid Change
NM_004836.7:c.439-170A= MANE Select	NP_004827.4:n.439-170A=
ENST00000303236.9:c.439-170A= MANE Select	ENSP00000307235.3:n.439-170A=
NM_001313915.1:c.-15-170A=	NP_001300844.1:n.-15-170A=
NM_001313915.2:c.-15-170A=	NP_001300844.1:n.-15-170A=
NM_004836.5:c.439-170A=	NP_004827.4:n.439-170A=
NM_004836.6:c.439-170A=	NP_004827.4:n.439-170A=
ENST00000303236.7:c.439-170A=	ENSP00000307235.3:n.439-170A=
ENST00000415570.1:c.-8A=	ENSP00000412076.1:n.-8A=
ENST00000419748.5:c.-15-170A=	ENSP00000408325.1:n.-15-170A=
ENST00000652099.1:c.437-170A=
ENST00000652423.1:c.*123-170A=	ENSP00000498948.1:n.*123-170A=
ENST00000652736.1:n.315-170A=
ENST00000682892.1:c.-15-170A=	ENSP00000507214.1:n.-15-170A=
XM_017005376.2:c.-442-170A=	XP_016860865.1:n.-442-170A=
XR_939749.1:n.648-170A=