Canonical Allele Identifier: CA352293352
Gene: KLHL40 HGNC NCBI

Linked Data

dbSNP Id: rs1362925761
MyVariant Identifiers: chr3:g.42729683C>T (hg19) chr3:g.42688191C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.42688191C>T , CM000665.2:g.42688191C>T GRCh38
NC_000003.11:g.42729683C>T , CM000665.1:g.42729683C>T GRCh37
NC_000003.10:g.42704687C>T NCBI36
NG_033035.1:g.7673C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000287777.5:c.1202C>T MANE Select ENSP00000287777.4:p.Pro401Leu
ENST00000287777.4:c.1202C>T ENSP00000287777.4:p.Pro401Leu
NM_152393.3:c.1202C>T NP_689606.2:p.Pro401Leu
XM_005264866.2:c.1202C>T XP_005264923.1:p.Pro401Leu
NM_152393.4:c.1202C>T MANE Select NP_689606.2:p.Pro401Leu
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