Canonical Allele Identifier: CA1548139268

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881695A= , CM000667.2:g.56881695A=	GRCh38
NC_000005.9:g.56177522A= , CM000667.1:g.56177522A=	GRCh37
NC_000005.8:g.56213279A=	NCBI36
NG_031884.1:g.71623A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2495A= MANE Select	ENSP00000382423.3:p.His832=
ENST00000399503.3:c.2495A=	ENSP00000382423.3:p.His832=
NM_005921.1:c.2495A=	NP_005912.1:p.His832=
XM_005248519.3:c.2117A=	XP_005248576.2:p.His706=
XM_011543406.1:c.2240A=	XP_011541708.1:p.His747=
XM_011543407.1:c.2216A=	XP_011541709.1:p.His739=
XM_011543408.1:c.2495A=	XP_011541710.1:p.His832=
XM_017009484.1:c.2084A=	XP_016864973.1:p.His695=
XM_017009485.1:c.2006A=	XP_016864974.1:p.His669=
XR_001742068.2:n.2526A=
NM_005921.2:c.2495A= MANE Select	NP_005912.1:p.His832=