Canonical Allele Identifier: CA352293394
Gene: KLHL40 HGNC NCBI

Linked Data

dbSNP Id: rs1697302861
MyVariant Identifiers: chr3:g.42729698G>T (hg19) chr3:g.42688206G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.42688206G>T , CM000665.2:g.42688206G>T GRCh38
NC_000003.11:g.42729698G>T , CM000665.1:g.42729698G>T GRCh37
NC_000003.10:g.42704702G>T NCBI36
NG_033035.1:g.7688G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000287777.5:c.1217G>T MANE Select ENSP00000287777.4:p.Gly406Val
ENST00000287777.4:c.1217G>T ENSP00000287777.4:p.Gly406Val
NM_152393.3:c.1217G>T NP_689606.2:p.Gly406Val
XM_005264866.2:c.1217G>T XP_005264923.1:p.Gly406Val
NM_152393.4:c.1217G>T MANE Select NP_689606.2:p.Gly406Val
Search 100 bp 5'
Search 100 bp 3'