Canonical Allele Identifier: CA1585511443
Gene: KLHL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137628350C= , CM000667.2:g.137628350C= GRCh38
NC_000005.9:g.136964039C= , CM000667.1:g.136964039C= GRCh37
NC_000005.8:g.136991938C= NCBI36
NG_032569.1:g.112741G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309755.9:c.1538G= MANE Select ENSP00000312397.4:p.Gly513=
ENST00000309755.8:c.1538G= ENSP00000312397.4:p.Gly513=
ENST00000447439.6:n.1594G=
ENST00000504208.5:c.*422G= ENSP00000423585.1:n.*422G=
ENST00000506491.5:c.1292G= ENSP00000424828.1:p.Gly431=
ENST00000506873.5:n.1061G=
ENST00000508657.5:c.1442G= ENSP00000422099.1:p.Gly481=
ENST00000509694.1:n.331G=
NM_001257194.1:c.1442G= NP_001244123.1:p.Gly481=
NM_001257195.1:c.1292G= NP_001244124.1:p.Gly431=
NM_017415.2:c.1538G= NP_059111.2:p.Gly513=
NM_017415.3:c.1538G= MANE Select NP_059111.2:p.Gly513=
NM_001257195.2:c.1292G= NP_001244124.1:p.Gly431=