Canonical Allele Identifier: CA361048470
Gene: KLHL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137639141A>C , CM000667.2:g.137639141A>C GRCh38
NC_000005.9:g.136974830A>C , CM000667.1:g.136974830A>C GRCh37
NC_000005.8:g.137002729A>C NCBI36
NG_032569.1:g.101950T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000309755.9:c.1031T>G MANE Select ENSP00000312397.4:p.Phe344Cys
ENST00000309755.8:c.1031T>G ENSP00000312397.4:p.Phe344Cys
ENST00000502381.1:n.618T>G
ENST00000504208.5:c.*335-10704T>G ENSP00000423585.1:n.*335-10704T>G
ENST00000505853.1:c.911T>G ENSP00000426173.1:p.Phe304Cys
ENST00000506491.5:c.785T>G ENSP00000424828.1:p.Phe262Cys
ENST00000506873.5:n.656T>G
ENST00000508657.5:c.935T>G ENSP00000422099.1:p.Phe312Cys
NM_001257194.1:c.935T>G NP_001244123.1:p.Phe312Cys
NM_001257195.1:c.785T>G NP_001244124.1:p.Phe262Cys
NM_017415.2:c.1031T>G NP_059111.2:p.Phe344Cys
NM_017415.3:c.1031T>G MANE Select NP_059111.2:p.Phe344Cys
NM_001257195.2:c.785T>G NP_001244124.1:p.Phe262Cys