Canonical Allele Identifier: CA1585497702
Gene: KLHL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137639129T= , CM000667.2:g.137639129T= GRCh38
NC_000005.9:g.136974818T= , CM000667.1:g.136974818T= GRCh37
NC_000005.8:g.137002717T= NCBI36
NG_032569.1:g.101962A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309755.9:c.1043A= MANE Select ENSP00000312397.4:p.His348=
ENST00000309755.8:c.1043A= ENSP00000312397.4:p.His348=
ENST00000502381.1:n.630A=
ENST00000504208.5:c.*335-10692A= ENSP00000423585.1:n.*335-10692A=
ENST00000505853.1:c.923A= ENSP00000426173.1:p.His308=
ENST00000506491.5:c.797A= ENSP00000424828.1:p.His266=
ENST00000506873.5:n.668A=
ENST00000508657.5:c.947A= ENSP00000422099.1:p.His316=
NM_001257194.1:c.947A= NP_001244123.1:p.His316=
NM_001257195.1:c.797A= NP_001244124.1:p.His266=
NM_017415.2:c.1043A= NP_059111.2:p.His348=
NM_017415.3:c.1043A= MANE Select NP_059111.2:p.His348=
NM_001257195.2:c.797A= NP_001244124.1:p.His266=