Canonical Allele Identifier: CA2373784046
Gene: CDH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61531896_61531899delinsTTAG , CM000682.2:g.61531896_61531899delinsTTAG GRCh38
NC_000020.10:g.60106952_60106955delinsTTAG , CM000682.1:g.60106952_60106955delinsTTAG GRCh37
NC_000020.9:g.59540347_59540350delinsTTAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.170-211667_170-211664delinsTTAG MANE Select ENSP00000484928.1:n.170-211667_170-211664delinsTTAG
ENST00000614565.4:c.170-211667_170-211664delinsTTAG ENSP00000484928.1:n.170-211667_170-211664delinsTTAG
NM_001252338.2:c.58+32404_58+32407delinsTTAG NP_001239267.1:n.58+32404_58+32407delinsTTAG
NM_001794.4:c.170-211667_170-211664delinsTTAG NP_001785.2:n.170-211667_170-211664delinsTTAG
NM_001794.5:c.170-211667_170-211664delinsTTAG MANE Select NP_001785.2:n.170-211667_170-211664delinsTTAG