Canonical Allele Identifier: CA361045653
Gene: KLHL3 HGNC NCBI

Linked Data

dbSNP Id: rs1425097046

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137628380A>G , CM000667.2:g.137628380A>G GRCh38
NC_000005.9:g.136964069A>G , CM000667.1:g.136964069A>G GRCh37
NC_000005.8:g.136991968A>G NCBI36
NG_032569.1:g.112711T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309755.9:c.1508T>C MANE Select ENSP00000312397.4:p.Val503Ala
ENST00000309755.8:c.1508T>C ENSP00000312397.4:p.Val503Ala
ENST00000447439.6:n.1564T>C
ENST00000504208.5:c.*392T>C ENSP00000423585.1:n.*392T>C
ENST00000506491.5:c.1262T>C ENSP00000424828.1:p.Val421Ala
ENST00000506873.5:n.1031T>C
ENST00000508657.5:c.1412T>C ENSP00000422099.1:p.Val471Ala
ENST00000509694.1:n.301T>C
NM_001257194.1:c.1412T>C NP_001244123.1:p.Val471Ala
NM_001257195.1:c.1262T>C NP_001244124.1:p.Val421Ala
NM_017415.2:c.1508T>C NP_059111.2:p.Val503Ala
NM_017415.3:c.1508T>C MANE Select NP_059111.2:p.Val503Ala
NM_001257195.2:c.1262T>C NP_001244124.1:p.Val421Ala