Canonical Allele Identifier: CA1585497556
Gene: KLHL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137639022G= , CM000667.2:g.137639022G= GRCh38
NC_000005.9:g.136974711G= , CM000667.1:g.136974711G= GRCh37
NC_000005.8:g.137002610G= NCBI36
NG_032569.1:g.102069C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309755.9:c.1150C= MANE Select ENSP00000312397.4:p.Arg384=
ENST00000309755.8:c.1150C= ENSP00000312397.4:p.Arg384=
ENST00000502381.1:n.737C=
ENST00000504208.5:c.*335-10585C= ENSP00000423585.1:n.*335-10585C=
ENST00000505853.1:c.1030C= ENSP00000426173.1:p.Arg344=
ENST00000506491.5:c.904C= ENSP00000424828.1:p.Arg302=
ENST00000506873.5:n.775C=
ENST00000508657.5:c.1054C= ENSP00000422099.1:p.Arg352=
NM_001257194.1:c.1054C= NP_001244123.1:p.Arg352=
NM_001257195.1:c.904C= NP_001244124.1:p.Arg302=
NM_017415.2:c.1150C= NP_059111.2:p.Arg384=
NM_017415.3:c.1150C= MANE Select NP_059111.2:p.Arg384=
NM_001257195.2:c.904C= NP_001244124.1:p.Arg302=