Canonical Allele Identifier: CA403986257
Gene: KEAP1 HGNC NCBI

Linked Data

dbSNP Id: rs2144590335

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10489753C>G , CM000681.2:g.10489753C>G GRCh38
NC_000019.9:g.10600429C>G , CM000681.1:g.10600429C>G GRCh37
NC_000019.8:g.10461429C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000171111.10:c.1426G>C MANE Select ENSP00000171111.4:p.Gly476Arg
ENST00000171111.9:c.1426G>C ENSP00000171111.4:p.Gly476Arg
ENST00000393623.6:c.1426G>C ENSP00000377245.1:p.Gly476Arg
ENST00000590593.1:c.305-385G>C
ENST00000592478.5:c.245G>C
NM_012289.3:c.1426G>C NP_036421.2:p.Gly476Arg
NM_203500.1:c.1426G>C NP_987096.1:p.Gly476Arg
XM_005260173.1:c.1426G>C XP_005260230.1:p.Gly476Arg
XM_005260174.1:c.1426G>C XP_005260231.1:p.Gly476Arg
XM_011528452.1:c.1426G>C XP_011526754.1:p.Gly476Arg
NM_203500.2:c.1426G>C MANE Select NP_987096.1:p.Gly476Arg
NM_012289.4:c.1426G>C NP_036421.2:p.Gly476Arg