Canonical Allele Identifier: CA1585497681
Gene: KLHL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137639109A= , CM000667.2:g.137639109A= GRCh38
NC_000005.9:g.136974798A= , CM000667.1:g.136974798A= GRCh37
NC_000005.8:g.137002697A= NCBI36
NG_032569.1:g.101982T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309755.9:c.1063T= MANE Select ENSP00000312397.4:p.Phe355=
ENST00000309755.8:c.1063T= ENSP00000312397.4:p.Phe355=
ENST00000502381.1:n.650T=
ENST00000504208.5:c.*335-10672T= ENSP00000423585.1:n.*335-10672T=
ENST00000505853.1:c.943T= ENSP00000426173.1:p.Phe315=
ENST00000506491.5:c.817T= ENSP00000424828.1:p.Phe273=
ENST00000506873.5:n.688T=
ENST00000508657.5:c.967T= ENSP00000422099.1:p.Phe323=
NM_001257194.1:c.967T= NP_001244123.1:p.Phe323=
NM_001257195.1:c.817T= NP_001244124.1:p.Phe273=
NM_017415.2:c.1063T= NP_059111.2:p.Phe355=
NM_017415.3:c.1063T= MANE Select NP_059111.2:p.Phe355=
NM_001257195.2:c.817T= NP_001244124.1:p.Phe273=