Canonical Allele Identifier: CA1548129229

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859832_56859835delinsCCTT , CM000667.2:g.56859832_56859835delinsCCTT	GRCh38
NC_000005.9:g.56155659_56155662delinsCCTT , CM000667.1:g.56155659_56155662delinsCCTT	GRCh37
NC_000005.8:g.56191416_56191419delinsCCTT	NCBI36
NG_031884.1:g.49760_49763delinsCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.751_754delinsCCTT MANE Select	ENSP00000382423.3:p.Pro251=
ENST00000399503.3:c.751_754delinsCCTT	ENSP00000382423.3:p.Pro251=
NM_005921.1:c.751_754delinsCCTT	NP_005912.1:p.Pro251=
XM_005248519.3:c.373_376delinsCCTT	XP_005248576.2:p.Pro125=
XM_011543406.1:c.496_499delinsCCTT	XP_011541708.1:p.Pro166=
XM_011543407.1:c.751_754delinsCCTT	XP_011541709.1:p.Pro251=
XM_011543408.1:c.751_754delinsCCTT	XP_011541710.1:p.Pro251=
XM_017009484.1:c.340_343delinsCCTT	XP_016864973.1:p.Pro114=
XM_017009485.1:c.262_265delinsCCTT	XP_016864974.1:p.Pro88=
XR_001742068.2:n.782_785delinsCCTT
NM_005921.2:c.751_754delinsCCTT MANE Select	NP_005912.1:p.Pro251=