Canonical Allele Identifier: CA1548139347

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881887C= , CM000667.2:g.56881887C=	GRCh38
NC_000005.9:g.56177714C= , CM000667.1:g.56177714C=	GRCh37
NC_000005.8:g.56213471C=	NCBI36
NG_031884.1:g.71815C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2687C= MANE Select	ENSP00000382423.3:p.Thr896=
ENST00000399503.3:c.2687C=	ENSP00000382423.3:p.Thr896=
NM_005921.1:c.2687C=	NP_005912.1:p.Thr896=
XM_005248519.3:c.2309C=	XP_005248576.2:p.Thr770=
XM_011543406.1:c.2432C=	XP_011541708.1:p.Thr811=
XM_011543407.1:c.2408C=	XP_011541709.1:p.Thr803=
XM_011543408.1:c.2687C=	XP_011541710.1:p.Thr896=
XM_017009484.1:c.2276C=	XP_016864973.1:p.Thr759=
XM_017009485.1:c.2198C=	XP_016864974.1:p.Thr733=
XR_001742068.2:n.2718C=
NM_005921.2:c.2687C= MANE Select	NP_005912.1:p.Thr896=