Canonical Allele Identifier: CA1548139178

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881453_56881454delinsCT , CM000667.2:g.56881453_56881454delinsCT	GRCh38
NC_000005.9:g.56177280_56177281delinsCT , CM000667.1:g.56177280_56177281delinsCT	GRCh37
NC_000005.8:g.56213037_56213038delinsCT	NCBI36
NG_031884.1:g.71381_71382delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2370-117_2370-116delinsCT MANE Select	ENSP00000382423.3:n.2370-117_2370-116delinsCT
ENST00000399503.3:c.2370-117_2370-116delinsCT	ENSP00000382423.3:n.2370-117_2370-116delinsCT
NM_005921.1:c.2370-117_2370-116delinsCT	NP_005912.1:n.2370-117_2370-116delinsCT
XM_005248519.3:c.1992-117_1992-116delinsCT	XP_005248576.2:n.1992-117_1992-116delinsCT
XM_011543406.1:c.2115-117_2115-116delinsCT	XP_011541708.1:n.2115-117_2115-116delinsCT
XM_011543407.1:c.2091-117_2091-116delinsCT	XP_011541709.1:n.2091-117_2091-116delinsCT
XM_011543408.1:c.2370-117_2370-116delinsCT	XP_011541710.1:n.2370-117_2370-116delinsCT
XM_017009484.1:c.1959-117_1959-116delinsCT	XP_016864973.1:n.1959-117_1959-116delinsCT
XM_017009485.1:c.1881-117_1881-116delinsCT	XP_016864974.1:n.1881-117_1881-116delinsCT
XR_001742068.2:n.2401-117_2401-116delinsCT
NM_005921.2:c.2370-117_2370-116delinsCT MANE Select	NP_005912.1:n.2370-117_2370-116delinsCT