Canonical Allele Identifier: CA1548136435

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875200A= , CM000667.2:g.56875200A=	GRCh38
NC_000005.9:g.56171027A= , CM000667.1:g.56171027A=	GRCh37
NC_000005.8:g.56206784A=	NCBI36
NG_031884.1:g.65128A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.1855A= MANE Select	ENSP00000382423.3:p.Thr619=
ENST00000399503.3:c.1855A=	ENSP00000382423.3:p.Thr619=
NM_005921.1:c.1855A=	NP_005912.1:p.Thr619=
XM_005248519.3:c.1477A=	XP_005248576.2:p.Thr493=
XM_011543406.1:c.1600A=	XP_011541708.1:p.Thr534=
XM_011543407.1:c.1686+2195A=	XP_011541709.1:n.1686+2195A=
XM_011543408.1:c.1855A=	XP_011541710.1:p.Thr619=
XM_017009484.1:c.1444A=	XP_016864973.1:p.Thr482=
XM_017009485.1:c.1366A=	XP_016864974.1:p.Thr456=
XR_001742068.2:n.1886A=
NM_005921.2:c.1855A= MANE Select	NP_005912.1:p.Thr619=