Canonical Allele Identifier: CA1548139285

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881750C= , CM000667.2:g.56881750C=	GRCh38
NC_000005.9:g.56177577C= , CM000667.1:g.56177577C=	GRCh37
NC_000005.8:g.56213334C=	NCBI36
NG_031884.1:g.71678C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2550C= MANE Select	ENSP00000382423.3:p.Thr850=
ENST00000399503.3:c.2550C=	ENSP00000382423.3:p.Thr850=
NM_005921.1:c.2550C=	NP_005912.1:p.Thr850=
XM_005248519.3:c.2172C=	XP_005248576.2:p.Thr724=
XM_011543406.1:c.2295C=	XP_011541708.1:p.Thr765=
XM_011543407.1:c.2271C=	XP_011541709.1:p.Thr757=
XM_011543408.1:c.2550C=	XP_011541710.1:p.Thr850=
XM_017009484.1:c.2139C=	XP_016864973.1:p.Thr713=
XM_017009485.1:c.2061C=	XP_016864974.1:p.Thr687=
XR_001742068.2:n.2581C=
NM_005921.2:c.2550C= MANE Select	NP_005912.1:p.Thr850=