Canonical Allele Identifier: CA1548139358

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881910T= , CM000667.2:g.56881910T=	GRCh38
NC_000005.9:g.56177737T= , CM000667.1:g.56177737T=	GRCh37
NC_000005.8:g.56213494T=	NCBI36
NG_031884.1:g.71838T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2710T= MANE Select	ENSP00000382423.3:p.Cys904=
ENST00000399503.3:c.2710T=	ENSP00000382423.3:p.Cys904=
NM_005921.1:c.2710T=	NP_005912.1:p.Cys904=
XM_005248519.3:c.2332T=	XP_005248576.2:p.Cys778=
XM_011543406.1:c.2455T=	XP_011541708.1:p.Cys819=
XM_011543407.1:c.2431T=	XP_011541709.1:p.Cys811=
XM_011543408.1:c.2710T=	XP_011541710.1:p.Cys904=
XM_017009484.1:c.2299T=	XP_016864973.1:p.Cys767=
XM_017009485.1:c.2221T=	XP_016864974.1:p.Cys741=
XR_001742068.2:n.2741T=
NM_005921.2:c.2710T= MANE Select	NP_005912.1:p.Cys904=