Canonical Allele Identifier: CA1548129199

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859770C= , CM000667.2:g.56859770C=	GRCh38
NC_000005.9:g.56155597C= , CM000667.1:g.56155597C=	GRCh37
NC_000005.8:g.56191354C=	NCBI36
NG_031884.1:g.49698C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.689C= MANE Select	ENSP00000382423.3:p.Ala230=
ENST00000399503.3:c.689C=	ENSP00000382423.3:p.Ala230=
NM_005921.1:c.689C=	NP_005912.1:p.Ala230=
XM_005248519.3:c.311C=	XP_005248576.2:p.Ala104=
XM_011543406.1:c.434C=	XP_011541708.1:p.Ala145=
XM_011543407.1:c.689C=	XP_011541709.1:p.Ala230=
XM_011543408.1:c.689C=	XP_011541710.1:p.Ala230=
XM_017009484.1:c.278C=	XP_016864973.1:p.Ala93=
XM_017009485.1:c.200C=	XP_016864974.1:p.Ala67=
XR_001742068.2:n.720C=
NM_005921.2:c.689C= MANE Select	NP_005912.1:p.Ala230=