Canonical Allele Identifier: CA1585511464
Gene: KLHL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137628400A= , CM000667.2:g.137628400A= GRCh38
NC_000005.9:g.136964089A= , CM000667.1:g.136964089A= GRCh37
NC_000005.8:g.136991988A= NCBI36
NG_032569.1:g.112691T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309755.9:c.1488T= MANE Select ENSP00000312397.4:p.Gly496=
ENST00000309755.8:c.1488T= ENSP00000312397.4:p.Gly496=
ENST00000447439.6:n.1544T=
ENST00000504208.5:c.*372T= ENSP00000423585.1:n.*372T=
ENST00000506491.5:c.1242T= ENSP00000424828.1:p.Gly414=
ENST00000506873.5:n.1011T=
ENST00000508657.5:c.1392T= ENSP00000422099.1:p.Gly464=
ENST00000509694.1:n.281T=
NM_001257194.1:c.1392T= NP_001244123.1:p.Gly464=
NM_001257195.1:c.1242T= NP_001244124.1:p.Gly414=
NM_017415.2:c.1488T= NP_059111.2:p.Gly496=
NM_017415.3:c.1488T= MANE Select NP_059111.2:p.Gly496=
NM_001257195.2:c.1242T= NP_001244124.1:p.Gly414=