Canonical Allele Identifier: CA352293362
Gene: KLHL40 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.42729688T>G (hg19) chr3:g.42688196T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.42688196T>G , CM000665.2:g.42688196T>G GRCh38
NC_000003.11:g.42729688T>G , CM000665.1:g.42729688T>G GRCh37
NC_000003.10:g.42704692T>G NCBI36
NG_033035.1:g.7678T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000287777.5:c.1207T>G MANE Select ENSP00000287777.4:p.Cys403Gly
ENST00000287777.4:c.1207T>G ENSP00000287777.4:p.Cys403Gly
NM_152393.3:c.1207T>G NP_689606.2:p.Cys403Gly
XM_005264866.2:c.1207T>G XP_005264923.1:p.Cys403Gly
NM_152393.4:c.1207T>G MANE Select NP_689606.2:p.Cys403Gly
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