Canonical Allele Identifier: CA2675417803
Gene: KLHL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137639785_137639788dup , CM000667.2:g.137639785_137639788dup GRCh38
NC_000005.9:g.136975474_136975477dup , CM000667.1:g.136975474_136975477dup GRCh37
NC_000005.8:g.137003373_137003376dup NCBI36
NG_032569.1:g.101303_101306dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000309755.9:c.1021+72_1021+75dup MANE Select ENSP00000312397.4:n.1021+72_1021+75dup
ENST00000309755.8:c.1021+72_1021+75dup ENSP00000312397.4:n.1021+72_1021+75dup
ENST00000502381.1:n.608+72_608+75dup
ENST00000504208.5:c.*335-11351_*335-11348dup ENSP00000423585.1:n.*335-11351_*335-11348dup
ENST00000505853.1:c.901+72_901+75dup ENSP00000426173.1:n.901+72_901+75dup
ENST00000506491.5:c.775+72_775+75dup ENSP00000424828.1:n.775+72_775+75dup
ENST00000506873.5:n.646+72_646+75dup
ENST00000508657.5:c.925+72_925+75dup ENSP00000422099.1:n.925+72_925+75dup
NM_001257194.1:c.925+72_925+75dup NP_001244123.1:n.925+72_925+75dup
NM_001257195.1:c.775+72_775+75dup NP_001244124.1:n.775+72_775+75dup
NM_017415.2:c.1021+72_1021+75dup NP_059111.2:n.1021+72_1021+75dup
NM_017415.3:c.1021+72_1021+75dup MANE Select NP_059111.2:n.1021+72_1021+75dup
NM_001257195.2:c.775+72_775+75dup NP_001244124.1:n.775+72_775+75dup