Canonical Allele Identifier: CA1585497685
Gene: KLHL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137639110C= , CM000667.2:g.137639110C= GRCh38
NC_000005.9:g.136974799C= , CM000667.1:g.136974799C= GRCh37
NC_000005.8:g.137002698C= NCBI36
NG_032569.1:g.101981G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309755.9:c.1062G= MANE Select ENSP00000312397.4:p.Gly354=
ENST00000309755.8:c.1062G= ENSP00000312397.4:p.Gly354=
ENST00000502381.1:n.649G=
ENST00000504208.5:c.*335-10673G= ENSP00000423585.1:n.*335-10673G=
ENST00000505853.1:c.942G= ENSP00000426173.1:p.Gly314=
ENST00000506491.5:c.816G= ENSP00000424828.1:p.Gly272=
ENST00000506873.5:n.687G=
ENST00000508657.5:c.966G= ENSP00000422099.1:p.Gly322=
NM_001257194.1:c.966G= NP_001244123.1:p.Gly322=
NM_001257195.1:c.816G= NP_001244124.1:p.Gly272=
NM_017415.2:c.1062G= NP_059111.2:p.Gly354=
NM_017415.3:c.1062G= MANE Select NP_059111.2:p.Gly354=
NM_001257195.2:c.816G= NP_001244124.1:p.Gly272=