Canonical Allele Identifier: CA1548139510

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882227C= , CM000667.2:g.56882227C=	GRCh38
NC_000005.9:g.56178054C= , CM000667.1:g.56178054C=	GRCh37
NC_000005.8:g.56213811C=	NCBI36
NG_031884.1:g.72155C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3027C= MANE Select	ENSP00000382423.3:p.Phe1009=
ENST00000399503.3:c.3027C=	ENSP00000382423.3:p.Phe1009=
NM_005921.1:c.3027C=	NP_005912.1:p.Phe1009=
XM_005248519.3:c.2649C=	XP_005248576.2:p.Phe883=
XM_011543406.1:c.2772C=	XP_011541708.1:p.Phe924=
XM_011543407.1:c.2748C=	XP_011541709.1:p.Phe916=
XM_011543408.1:c.3027C=	XP_011541710.1:p.Phe1009=
XM_017009484.1:c.2616C=	XP_016864973.1:p.Phe872=
XM_017009485.1:c.2538C=	XP_016864974.1:p.Phe846=
XR_001742068.2:n.3058C=
NM_005921.2:c.3027C= MANE Select	NP_005912.1:p.Phe1009=