Canonical Allele Identifier: CA1585511428
Gene: KLHL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137628317T= , CM000667.2:g.137628317T= GRCh38
NC_000005.9:g.136964006T= , CM000667.1:g.136964006T= GRCh37
NC_000005.8:g.136991905T= NCBI36
NG_032569.1:g.112774A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309755.9:c.1571A= MANE Select ENSP00000312397.4:p.Asn524=
ENST00000309755.8:c.1571A= ENSP00000312397.4:p.Asn524=
ENST00000447439.6:n.1627A=
ENST00000504208.5:c.*455A= ENSP00000423585.1:n.*455A=
ENST00000506491.5:c.1325A= ENSP00000424828.1:p.Asn442=
ENST00000506873.5:n.1094A=
ENST00000508657.5:c.1475A= ENSP00000422099.1:p.Asn492=
ENST00000509694.1:n.364A=
NM_001257194.1:c.1475A= NP_001244123.1:p.Asn492=
NM_001257195.1:c.1325A= NP_001244124.1:p.Asn442=
NM_017415.2:c.1571A= NP_059111.2:p.Asn524=
NM_017415.3:c.1571A= MANE Select NP_059111.2:p.Asn524=
NM_001257195.2:c.1325A= NP_001244124.1:p.Asn442=