Canonical Allele Identifier: CA1585497628
Gene: KLHL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137639067C= , CM000667.2:g.137639067C= GRCh38
NC_000005.9:g.136974756C= , CM000667.1:g.136974756C= GRCh37
NC_000005.8:g.137002655C= NCBI36
NG_032569.1:g.102024G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309755.9:c.1105G= MANE Select ENSP00000312397.4:p.Gly369=
ENST00000309755.8:c.1105G= ENSP00000312397.4:p.Gly369=
ENST00000502381.1:n.692G=
ENST00000504208.5:c.*335-10630G= ENSP00000423585.1:n.*335-10630G=
ENST00000505853.1:c.985G= ENSP00000426173.1:p.Gly329=
ENST00000506491.5:c.859G= ENSP00000424828.1:p.Gly287=
ENST00000506873.5:n.730G=
ENST00000508657.5:c.1009G= ENSP00000422099.1:p.Gly337=
NM_001257194.1:c.1009G= NP_001244123.1:p.Gly337=
NM_001257195.1:c.859G= NP_001244124.1:p.Gly287=
NM_017415.2:c.1105G= NP_059111.2:p.Gly369=
NM_017415.3:c.1105G= MANE Select NP_059111.2:p.Gly369=
NM_001257195.2:c.859G= NP_001244124.1:p.Gly287=