Canonical Allele Identifier: CA1548139212

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881541A= , CM000667.2:g.56881541A=	GRCh38
NC_000005.9:g.56177368A= , CM000667.1:g.56177368A=	GRCh37
NC_000005.8:g.56213125A=	NCBI36
NG_031884.1:g.71469A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2370-29A= MANE Select	ENSP00000382423.3:n.2370-29A=
ENST00000399503.3:c.2370-29A=	ENSP00000382423.3:n.2370-29A=
NM_005921.1:c.2370-29A=	NP_005912.1:n.2370-29A=
XM_005248519.3:c.1992-29A=	XP_005248576.2:n.1992-29A=
XM_011543406.1:c.2115-29A=	XP_011541708.1:n.2115-29A=
XM_011543407.1:c.2091-29A=	XP_011541709.1:n.2091-29A=
XM_011543408.1:c.2370-29A=	XP_011541710.1:n.2370-29A=
XM_017009484.1:c.1959-29A=	XP_016864973.1:n.1959-29A=
XM_017009485.1:c.1881-29A=	XP_016864974.1:n.1881-29A=
XR_001742068.2:n.2401-29A=
NM_005921.2:c.2370-29A= MANE Select	NP_005912.1:n.2370-29A=