Canonical Allele Identifier: CA1548139383

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881979A= , CM000667.2:g.56881979A=	GRCh38
NC_000005.9:g.56177806A= , CM000667.1:g.56177806A=	GRCh37
NC_000005.8:g.56213563A=	NCBI36
NG_031884.1:g.71907A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2779A= MANE Select	ENSP00000382423.3:p.Ile927=
ENST00000399503.3:c.2779A=	ENSP00000382423.3:p.Ile927=
NM_005921.1:c.2779A=	NP_005912.1:p.Ile927=
XM_005248519.3:c.2401A=	XP_005248576.2:p.Ile801=
XM_011543406.1:c.2524A=	XP_011541708.1:p.Ile842=
XM_011543407.1:c.2500A=	XP_011541709.1:p.Ile834=
XM_011543408.1:c.2779A=	XP_011541710.1:p.Ile927=
XM_017009484.1:c.2368A=	XP_016864973.1:p.Ile790=
XM_017009485.1:c.2290A=	XP_016864974.1:p.Ile764=
XR_001742068.2:n.2810A=
NM_005921.2:c.2779A= MANE Select	NP_005912.1:p.Ile927=