Canonical Allele Identifier: CA1585515938
Gene: KLHL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137638979G= , CM000667.2:g.137638979G= GRCh38
NC_000005.9:g.136974668G= , CM000667.1:g.136974668G= GRCh37
NC_000005.8:g.137002567G= NCBI36
NG_032569.1:g.102112C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309755.9:c.1193C= MANE Select ENSP00000312397.4:p.Ala398=
ENST00000309755.8:c.1193C= ENSP00000312397.4:p.Ala398=
ENST00000502381.1:n.780C=
ENST00000504208.5:c.*335-10542C= ENSP00000423585.1:n.*335-10542C=
ENST00000505853.1:c.1073C= ENSP00000426173.1:p.Ala358=
ENST00000506491.5:c.947C= ENSP00000424828.1:p.Ala316=
ENST00000506873.5:n.818C=
ENST00000508657.5:c.1097C= ENSP00000422099.1:p.Ala366=
NM_001257194.1:c.1097C= NP_001244123.1:p.Ala366=
NM_001257195.1:c.947C= NP_001244124.1:p.Ala316=
NM_017415.2:c.1193C= NP_059111.2:p.Ala398=
NM_017415.3:c.1193C= MANE Select NP_059111.2:p.Ala398=
NM_001257195.2:c.947C= NP_001244124.1:p.Ala316=