Canonical Allele Identifier: CA1548139381

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881977A= , CM000667.2:g.56881977A=	GRCh38
NC_000005.9:g.56177804A= , CM000667.1:g.56177804A=	GRCh37
NC_000005.8:g.56213561A=	NCBI36
NG_031884.1:g.71905A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2777A= MANE Select	ENSP00000382423.3:p.Asp926=
ENST00000399503.3:c.2777A=	ENSP00000382423.3:p.Asp926=
NM_005921.1:c.2777A=	NP_005912.1:p.Asp926=
XM_005248519.3:c.2399A=	XP_005248576.2:p.Asp800=
XM_011543406.1:c.2522A=	XP_011541708.1:p.Asp841=
XM_011543407.1:c.2498A=	XP_011541709.1:p.Asp833=
XM_011543408.1:c.2777A=	XP_011541710.1:p.Asp926=
XM_017009484.1:c.2366A=	XP_016864973.1:p.Asp789=
XM_017009485.1:c.2288A=	XP_016864974.1:p.Asp763=
XR_001742068.2:n.2808A=
NM_005921.2:c.2777A= MANE Select	NP_005912.1:p.Asp926=