Canonical Allele Identifier: CA9934888
Gene: CDH4 HGNC NCBI

Linked Data

dbSNP Id: rs371571270

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61928281G>T , CM000682.2:g.61928281G>T GRCh38
NC_000020.10:g.60503339G>T , CM000682.1:g.60503339G>T GRCh37
NC_000020.9:g.59936734G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.1863G>T MANE Select ENSP00000484928.1:p.Gln621His
ENST00000543233.2:c.1641G>T ENSP00000443301.1:p.Gln547His
ENST00000611855.4:c.1581G>T ENSP00000480844.1:p.Gln527His
ENST00000614565.4:c.1863G>T ENSP00000484928.1:p.Gln621His
NM_001252338.2:c.1752G>T NP_001239267.1:p.Gln584His
NM_001252339.2:c.1641G>T NP_001239268.1:p.Gln547His
NM_001794.4:c.1863G>T NP_001785.2:p.Gln621His
NM_001794.5:c.1863G>T MANE Select NP_001785.2:p.Gln621His
NM_001252339.3:c.1641G>T NP_001239268.1:p.Gln547His