Canonical Allele Identifier: CA1548139222

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881559T= , CM000667.2:g.56881559T=	GRCh38
NC_000005.9:g.56177386T= , CM000667.1:g.56177386T=	GRCh37
NC_000005.8:g.56213143T=	NCBI36
NG_031884.1:g.71487T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2370-11T= MANE Select	ENSP00000382423.3:n.2370-11T=
ENST00000399503.3:c.2370-11T=	ENSP00000382423.3:n.2370-11T=
NM_005921.1:c.2370-11T=	NP_005912.1:n.2370-11T=
XM_005248519.3:c.1992-11T=	XP_005248576.2:n.1992-11T=
XM_011543406.1:c.2115-11T=	XP_011541708.1:n.2115-11T=
XM_011543407.1:c.2091-11T=	XP_011541709.1:n.2091-11T=
XM_011543408.1:c.2370-11T=	XP_011541710.1:n.2370-11T=
XM_017009484.1:c.1959-11T=	XP_016864973.1:n.1959-11T=
XM_017009485.1:c.1881-11T=	XP_016864974.1:n.1881-11T=
XR_001742068.2:n.2401-11T=
NM_005921.2:c.2370-11T= MANE Select	NP_005912.1:n.2370-11T=