Canonical Allele Identifier: CA1585511476
Gene: KLHL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137628437C= , CM000667.2:g.137628437C= GRCh38
NC_000005.9:g.136964126C= , CM000667.1:g.136964126C= GRCh37
NC_000005.8:g.136992025C= NCBI36
NG_032569.1:g.112654G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309755.9:c.1451G= MANE Select ENSP00000312397.4:p.Gly484=
ENST00000309755.8:c.1451G= ENSP00000312397.4:p.Gly484=
ENST00000447439.6:n.1507G=
ENST00000504208.5:c.*335G= ENSP00000423585.1:n.*335G=
ENST00000506491.5:c.1205G= ENSP00000424828.1:p.Gly402=
ENST00000506873.5:n.974G=
ENST00000508657.5:c.1355G= ENSP00000422099.1:p.Gly452=
ENST00000509694.1:n.244G=
NM_001257194.1:c.1355G= NP_001244123.1:p.Gly452=
NM_001257195.1:c.1205G= NP_001244124.1:p.Gly402=
NM_017415.2:c.1451G= NP_059111.2:p.Gly484=
NM_017415.3:c.1451G= MANE Select NP_059111.2:p.Gly484=
NM_001257195.2:c.1205G= NP_001244124.1:p.Gly402=