Canonical Allele Identifier: CA1548136469

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875275G= , CM000667.2:g.56875275G=	GRCh38
NC_000005.9:g.56171102G= , CM000667.1:g.56171102G=	GRCh37
NC_000005.8:g.56206859G=	NCBI36
NG_031884.1:g.65203G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1930G= MANE Select	ENSP00000382423.3:p.Ala644=
ENST00000399503.3:c.1930G=	ENSP00000382423.3:p.Ala644=
NM_005921.1:c.1930G=	NP_005912.1:p.Ala644=
XM_005248519.3:c.1552G=	XP_005248576.2:p.Ala518=
XM_011543406.1:c.1675G=	XP_011541708.1:p.Ala559=
XM_011543407.1:c.1686+2270G=	XP_011541709.1:n.1686+2270G=
XM_011543408.1:c.1930G=	XP_011541710.1:p.Ala644=
XM_017009484.1:c.1519G=	XP_016864973.1:p.Ala507=
XM_017009485.1:c.1441G=	XP_016864974.1:p.Ala481=
XR_001742068.2:n.1961G=
NM_005921.2:c.1930G= MANE Select	NP_005912.1:p.Ala644=