Canonical Allele Identifier: CA1019115142
Gene: CDH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61637438C>A , CM000682.2:g.61637438C>A GRCh38
NC_000020.10:g.60212494C>A , CM000682.1:g.60212494C>A GRCh37
NC_000020.9:g.59645889C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.170-106125C>A MANE Select ENSP00000484928.1:n.170-106125C>A
ENST00000543233.2:c.-54+37449C>A ENSP00000443301.1:n.-54+37449C>A
ENST00000611855.4:c.49+66695C>A ENSP00000480844.1:n.49+66695C>A
ENST00000614565.4:c.170-106125C>A ENSP00000484928.1:n.170-106125C>A
NM_001252338.2:c.59-106125C>A NP_001239267.1:n.59-106125C>A
NM_001252339.2:c.-54+37449C>A NP_001239268.1:n.-54+37449C>A
NM_001794.4:c.170-106125C>A NP_001785.2:n.170-106125C>A
NM_001794.5:c.170-106125C>A MANE Select NP_001785.2:n.170-106125C>A
NM_001252339.3:c.-54+37449C>A NP_001239268.1:n.-54+37449C>A