Canonical Allele Identifier: CA489666957

Gene: EIF2AK4

Linked Data

• MyVariant Identifiers: chr15:g.40313132A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40020931A>C , CM000677.2:g.40020931A>C	GRCh38
NC_000015.9:g.40313132A>C , CM000677.1:g.40313132A>C	GRCh37
NC_000015.8:g.38100424A>C	NCBI36
NG_034053.1:g.91808A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000263791.10:c.4206A>C MANE Select	ENSP00000263791.5:p.Val1402=
ENST00000263791.9:c.4206A>C	ENSP00000263791.5:p.Val1402=
ENST00000558557.1:n.1198A>C
ENST00000558629.5:n.3123A>C
ENST00000558743.1:n.406A>C
ENST00000560855.5:c.3538A>C
NM_001013703.3:c.4206A>C	NP_001013725.2:p.Val1402=
XM_005254392.1:c.4206A>C	XP_005254449.1:p.Val1402=
XM_011521599.1:c.4206A>C	XP_011519901.1:p.Val1402=
XM_011521600.1:c.4035A>C	XP_011519902.1:p.Val1345=
XM_005254392.3:c.4206A>C	XP_005254449.1:p.Val1402=
XM_011521599.2:c.4206A>C	XP_011519901.1:p.Val1402=
XM_011521600.3:c.4035A>C	XP_011519902.1:p.Val1345=
XM_017022219.2:c.4035A>C	XP_016877708.1:p.Val1345=
NM_001013703.4:c.4206A>C MANE Select	NP_001013725.2:p.Val1402=