Canonical Allele Identifier: CA403986124
Gene: KEAP1 HGNC NCBI

Linked Data

dbSNP Id: rs2144590205
COSMIC: COSM710199

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10489741C>A , CM000681.2:g.10489741C>A GRCh38
NC_000019.9:g.10600417C>A , CM000681.1:g.10600417C>A GRCh37
NC_000019.8:g.10461417C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000171111.10:c.1438G>T MANE Select ENSP00000171111.4:p.Gly480Trp
ENST00000171111.9:c.1438G>T ENSP00000171111.4:p.Gly480Trp
ENST00000393623.6:c.1438G>T ENSP00000377245.1:p.Gly480Trp
ENST00000590593.1:c.305-373G>T
ENST00000592478.5:c.257G>T
NM_012289.3:c.1438G>T NP_036421.2:p.Gly480Trp
NM_203500.1:c.1438G>T NP_987096.1:p.Gly480Trp
XM_005260173.1:c.1438G>T XP_005260230.1:p.Gly480Trp
XM_005260174.1:c.1438G>T XP_005260231.1:p.Gly480Trp
XM_011528452.1:c.1438G>T XP_011526754.1:p.Gly480Trp
NM_203500.2:c.1438G>T MANE Select NP_987096.1:p.Gly480Trp
NM_012289.4:c.1438G>T NP_036421.2:p.Gly480Trp