Canonical Allele Identifier: CA446560985
Gene: KLHL3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.136974685G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137638996G>C , CM000667.2:g.137638996G>C GRCh38
NC_000005.9:g.136974685G>C , CM000667.1:g.136974685G>C GRCh37
NC_000005.8:g.137002584G>C NCBI36
NG_032569.1:g.102095C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000309755.9:c.1176C>G MANE Select ENSP00000312397.4:p.Leu392=
ENST00000309755.8:c.1176C>G ENSP00000312397.4:p.Leu392=
ENST00000502381.1:n.763C>G
ENST00000504208.5:c.*335-10559C>G ENSP00000423585.1:n.*335-10559C>G
ENST00000505853.1:c.1056C>G ENSP00000426173.1:p.Leu352=
ENST00000506491.5:c.930C>G ENSP00000424828.1:p.Leu310=
ENST00000506873.5:n.801C>G
ENST00000508657.5:c.1080C>G ENSP00000422099.1:p.Leu360=
NM_001257194.1:c.1080C>G NP_001244123.1:p.Leu360=
NM_001257195.1:c.930C>G NP_001244124.1:p.Leu310=
NM_017415.2:c.1176C>G NP_059111.2:p.Leu392=
NM_017415.3:c.1176C>G MANE Select NP_059111.2:p.Leu392=
NM_001257195.2:c.930C>G NP_001244124.1:p.Leu310=