Canonical Allele Identifier: CA1548136397

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875102G= , CM000667.2:g.56875102G=	GRCh38
NC_000005.9:g.56170929G= , CM000667.1:g.56170929G=	GRCh37
NC_000005.8:g.56206686G=	NCBI36
NG_031884.1:g.65030G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1757G= MANE Select	ENSP00000382423.3:p.Arg586=
ENST00000399503.3:c.1757G=	ENSP00000382423.3:p.Arg586=
NM_005921.1:c.1757G=	NP_005912.1:p.Arg586=
XM_005248519.3:c.1379G=	XP_005248576.2:p.Arg460=
XM_011543406.1:c.1502G=	XP_011541708.1:p.Arg501=
XM_011543407.1:c.1686+2097G=	XP_011541709.1:n.1686+2097G=
XM_011543408.1:c.1757G=	XP_011541710.1:p.Arg586=
XM_017009484.1:c.1346G=	XP_016864973.1:p.Arg449=
XM_017009485.1:c.1268G=	XP_016864974.1:p.Arg423=
XR_001742068.2:n.1788G=
NM_005921.2:c.1757G= MANE Select	NP_005912.1:p.Arg586=