Canonical Allele Identifier: CA1585497507
Gene: KLHL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137638993A= , CM000667.2:g.137638993A= GRCh38
NC_000005.9:g.136974682A= , CM000667.1:g.136974682A= GRCh37
NC_000005.8:g.137002581A= NCBI36
NG_032569.1:g.102098T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309755.9:c.1179T= MANE Select ENSP00000312397.4:p.Asn393=
ENST00000309755.8:c.1179T= ENSP00000312397.4:p.Asn393=
ENST00000502381.1:n.766T=
ENST00000504208.5:c.*335-10556T= ENSP00000423585.1:n.*335-10556T=
ENST00000505853.1:c.1059T= ENSP00000426173.1:p.Asn353=
ENST00000506491.5:c.933T= ENSP00000424828.1:p.Asn311=
ENST00000506873.5:n.804T=
ENST00000508657.5:c.1083T= ENSP00000422099.1:p.Asn361=
NM_001257194.1:c.1083T= NP_001244123.1:p.Asn361=
NM_001257195.1:c.933T= NP_001244124.1:p.Asn311=
NM_017415.2:c.1179T= NP_059111.2:p.Asn393=
NM_017415.3:c.1179T= MANE Select NP_059111.2:p.Asn393=
NM_001257195.2:c.933T= NP_001244124.1:p.Asn311=