Canonical Allele Identifier: CA1548129152

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859659A= , CM000667.2:g.56859659A=	GRCh38
NC_000005.9:g.56155486A= , CM000667.1:g.56155486A=	GRCh37
NC_000005.8:g.56191243A=	NCBI36
NG_031884.1:g.49587A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.634-56A= MANE Select	ENSP00000382423.3:n.634-56A=
ENST00000399503.3:c.634-56A=	ENSP00000382423.3:n.634-56A=
NM_005921.1:c.634-56A=	NP_005912.1:n.634-56A=
XM_005248519.3:c.256-56A=	XP_005248576.2:n.256-56A=
XM_011543406.1:c.379-56A=	XP_011541708.1:n.379-56A=
XM_011543407.1:c.634-56A=	XP_011541709.1:n.634-56A=
XM_011543408.1:c.634-56A=	XP_011541710.1:n.634-56A=
XM_017009484.1:c.223-56A=	XP_016864973.1:n.223-56A=
XM_017009485.1:c.145-56A=	XP_016864974.1:n.145-56A=
XR_001742068.2:n.665-56A=
NM_005921.2:c.634-56A= MANE Select	NP_005912.1:n.634-56A=