Canonical Allele Identifier: CA1548129198

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859767C= , CM000667.2:g.56859767C=	GRCh38
NC_000005.9:g.56155594C= , CM000667.1:g.56155594C=	GRCh37
NC_000005.8:g.56191351C=	NCBI36
NG_031884.1:g.49695C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.686C= MANE Select	ENSP00000382423.3:p.Ala229=
ENST00000399503.3:c.686C=	ENSP00000382423.3:p.Ala229=
NM_005921.1:c.686C=	NP_005912.1:p.Ala229=
XM_005248519.3:c.308C=	XP_005248576.2:p.Ala103=
XM_011543406.1:c.431C=	XP_011541708.1:p.Ala144=
XM_011543407.1:c.686C=	XP_011541709.1:p.Ala229=
XM_011543408.1:c.686C=	XP_011541710.1:p.Ala229=
XM_017009484.1:c.275C=	XP_016864973.1:p.Ala92=
XM_017009485.1:c.197C=	XP_016864974.1:p.Ala66=
XR_001742068.2:n.717C=
NM_005921.2:c.686C= MANE Select	NP_005912.1:p.Ala229=