Canonical Allele Identifier: CA9934874
Gene: CDH4 HGNC NCBI

Linked Data

dbSNP Id: rs753137381

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61928207G>A , CM000682.2:g.61928207G>A GRCh38
NC_000020.10:g.60503265G>A , CM000682.1:g.60503265G>A GRCh37
NC_000020.9:g.59936660G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.1789G>A MANE Select ENSP00000484928.1:p.Gly597Ser
ENST00000543233.2:c.1567G>A ENSP00000443301.1:p.Gly523Ser
ENST00000611855.4:c.1507G>A ENSP00000480844.1:p.Gly503Ser
ENST00000614565.4:c.1789G>A ENSP00000484928.1:p.Gly597Ser
NM_001252338.2:c.1678G>A NP_001239267.1:p.Gly560Ser
NM_001252339.2:c.1567G>A NP_001239268.1:p.Gly523Ser
NM_001794.4:c.1789G>A NP_001785.2:p.Gly597Ser
NM_001794.5:c.1789G>A MANE Select NP_001785.2:p.Gly597Ser
NM_001252339.3:c.1567G>A NP_001239268.1:p.Gly523Ser