Canonical Allele Identifier: CA1548139519

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882251A= , CM000667.2:g.56882251A=	GRCh38
NC_000005.9:g.56178078A= , CM000667.1:g.56178078A=	GRCh37
NC_000005.8:g.56213835A=	NCBI36
NG_031884.1:g.72179A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3051A= MANE Select	ENSP00000382423.3:p.Ala1017=
ENST00000399503.3:c.3051A=	ENSP00000382423.3:p.Ala1017=
NM_005921.1:c.3051A=	NP_005912.1:p.Ala1017=
XM_005248519.3:c.2673A=	XP_005248576.2:p.Ala891=
XM_011543406.1:c.2796A=	XP_011541708.1:p.Ala932=
XM_011543407.1:c.2772A=	XP_011541709.1:p.Ala924=
XM_011543408.1:c.3051A=	XP_011541710.1:p.Ala1017=
XM_017009484.1:c.2640A=	XP_016864973.1:p.Ala880=
XM_017009485.1:c.2562A=	XP_016864974.1:p.Ala854=
XR_001742068.2:n.3082A=
NM_005921.2:c.3051A= MANE Select	NP_005912.1:p.Ala1017=