Canonical Allele Identifier: CA1548136442

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875215C= , CM000667.2:g.56875215C=	GRCh38
NC_000005.9:g.56171042C= , CM000667.1:g.56171042C=	GRCh37
NC_000005.8:g.56206799C=	NCBI36
NG_031884.1:g.65143C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1870C= MANE Select	ENSP00000382423.3:p.Gln624=
ENST00000399503.3:c.1870C=	ENSP00000382423.3:p.Gln624=
NM_005921.1:c.1870C=	NP_005912.1:p.Gln624=
XM_005248519.3:c.1492C=	XP_005248576.2:p.Gln498=
XM_011543406.1:c.1615C=	XP_011541708.1:p.Gln539=
XM_011543407.1:c.1686+2210C=	XP_011541709.1:n.1686+2210C=
XM_011543408.1:c.1870C=	XP_011541710.1:p.Gln624=
XM_017009484.1:c.1459C=	XP_016864973.1:p.Gln487=
XM_017009485.1:c.1381C=	XP_016864974.1:p.Gln461=
XR_001742068.2:n.1901C=
NM_005921.2:c.1870C= MANE Select	NP_005912.1:p.Gln624=