Canonical Allele Identifier: CA1548129206

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859788T= , CM000667.2:g.56859788T=	GRCh38
NC_000005.9:g.56155615T= , CM000667.1:g.56155615T=	GRCh37
NC_000005.8:g.56191372T=	NCBI36
NG_031884.1:g.49716T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.707T= MANE Select	ENSP00000382423.3:p.Val236=
ENST00000399503.3:c.707T=	ENSP00000382423.3:p.Val236=
NM_005921.1:c.707T=	NP_005912.1:p.Val236=
XM_005248519.3:c.329T=	XP_005248576.2:p.Val110=
XM_011543406.1:c.452T=	XP_011541708.1:p.Val151=
XM_011543407.1:c.707T=	XP_011541709.1:p.Val236=
XM_011543408.1:c.707T=	XP_011541710.1:p.Val236=
XM_017009484.1:c.296T=	XP_016864973.1:p.Val99=
XM_017009485.1:c.218T=	XP_016864974.1:p.Val73=
XR_001742068.2:n.738T=
NM_005921.2:c.707T= MANE Select	NP_005912.1:p.Val236=