Canonical Allele Identifier: CA1548128119

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56857443A= , CM000667.2:g.56857443A=	GRCh38
NC_000005.9:g.56153270A= , CM000667.1:g.56153270A=	GRCh37
NC_000005.8:g.56189027A=	NCBI36
NG_031884.1:g.47371A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.633+693A= MANE Select	ENSP00000382423.3:n.633+693A=
ENST00000399503.3:c.633+693A=	ENSP00000382423.3:n.633+693A=
NM_005921.1:c.633+693A=	NP_005912.1:n.633+693A=
XM_005248519.3:c.255+693A=	XP_005248576.2:n.255+693A=
XM_011543406.1:c.378+693A=	XP_011541708.1:n.378+693A=
XM_011543407.1:c.633+693A=	XP_011541709.1:n.633+693A=
XM_011543408.1:c.633+693A=	XP_011541710.1:n.633+693A=
XM_017009484.1:c.222+693A=	XP_016864973.1:n.222+693A=
XM_017009485.1:c.144+693A=	XP_016864974.1:n.144+693A=
XR_001742068.2:n.664+693A=
NM_005921.2:c.633+693A= MANE Select	NP_005912.1:n.633+693A=