Canonical Allele Identifier: CA2171582527

Gene: EIF2AK4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40016741T= , CM000677.2:g.40016741T=	GRCh38
NC_000015.9:g.40308942T= , CM000677.1:g.40308942T=	GRCh37
NC_000015.8:g.38096234T=	NCBI36
NG_034053.1:g.87618T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263791.10:c.3930+69T= MANE Select	ENSP00000263791.5:n.3930+69T=
ENST00000263791.9:c.3930+69T=	ENSP00000263791.5:n.3930+69T=
ENST00000558557.1:n.923-367T=
ENST00000558629.5:n.2847+69T=
ENST00000560855.5:c.3262+69T=
NM_001013703.3:c.3930+69T=	NP_001013725.2:n.3930+69T=
XM_005254392.1:c.3930+69T=	XP_005254449.1:n.3930+69T=
XM_011521599.1:c.3930+69T=	XP_011519901.1:n.3930+69T=
XM_011521600.1:c.3760-367T=	XP_011519902.1:n.3760-367T=
XM_005254392.3:c.3930+69T=	XP_005254449.1:n.3930+69T=
XM_011521599.2:c.3930+69T=	XP_011519901.1:n.3930+69T=
XM_011521600.3:c.3760-367T=	XP_011519902.1:n.3760-367T=
XM_017022219.2:c.3760-367T=	XP_016877708.1:n.3760-367T=
NM_001013703.4:c.3930+69T= MANE Select	NP_001013725.2:n.3930+69T=