Canonical Allele Identifier: CA1585511471
Gene: KLHL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137628419C= , CM000667.2:g.137628419C= GRCh38
NC_000005.9:g.136964108C= , CM000667.1:g.136964108C= GRCh37
NC_000005.8:g.136992007C= NCBI36
NG_032569.1:g.112672G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309755.9:c.1469G= MANE Select ENSP00000312397.4:p.Gly490=
ENST00000309755.8:c.1469G= ENSP00000312397.4:p.Gly490=
ENST00000447439.6:n.1525G=
ENST00000504208.5:c.*353G= ENSP00000423585.1:n.*353G=
ENST00000506491.5:c.1223G= ENSP00000424828.1:p.Gly408=
ENST00000506873.5:n.992G=
ENST00000508657.5:c.1373G= ENSP00000422099.1:p.Gly458=
ENST00000509694.1:n.262G=
NM_001257194.1:c.1373G= NP_001244123.1:p.Gly458=
NM_001257195.1:c.1223G= NP_001244124.1:p.Gly408=
NM_017415.2:c.1469G= NP_059111.2:p.Gly490=
NM_017415.3:c.1469G= MANE Select NP_059111.2:p.Gly490=
NM_001257195.2:c.1223G= NP_001244124.1:p.Gly408=