Canonical Allele Identifier: CA1548129264

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859910G= , CM000667.2:g.56859910G=	GRCh38
NC_000005.9:g.56155737G= , CM000667.1:g.56155737G=	GRCh37
NC_000005.8:g.56191494G=	NCBI36
NG_031884.1:g.49838G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.829G= MANE Select	ENSP00000382423.3:p.Val277=
ENST00000399503.3:c.829G=	ENSP00000382423.3:p.Val277=
NM_005921.1:c.829G=	NP_005912.1:p.Val277=
XM_005248519.3:c.451G=	XP_005248576.2:p.Val151=
XM_011543406.1:c.574G=	XP_011541708.1:p.Val192=
XM_011543407.1:c.829G=	XP_011541709.1:p.Val277=
XM_011543408.1:c.829G=	XP_011541710.1:p.Val277=
XM_017009484.1:c.418G=	XP_016864973.1:p.Val140=
XM_017009485.1:c.340G=	XP_016864974.1:p.Val114=
XR_001742068.2:n.860G=
NM_005921.2:c.829G= MANE Select	NP_005912.1:p.Val277=