Canonical Allele Identifier: CA317411401
Gene: CDH4 HGNC NCBI

Linked Data

dbSNP Id: rs904325682
gnomAD v3: 20-61531705-C-T
gnomAD v4: 20-61531705-C-T
MyVariant Identifiers: chr20:g.60106761C>T (hg19) chr20:g.61531705C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61531705C>T , CM000682.2:g.61531705C>T GRCh38
NC_000020.10:g.60106761C>T , CM000682.1:g.60106761C>T GRCh37
NC_000020.9:g.59540156C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.170-211858C>T MANE Select ENSP00000484928.1:n.170-211858C>T
ENST00000614565.4:c.170-211858C>T ENSP00000484928.1:n.170-211858C>T
NM_001252338.2:c.58+32213C>T NP_001239267.1:n.58+32213C>T
NM_001794.4:c.170-211858C>T NP_001785.2:n.170-211858C>T
NM_001794.5:c.170-211858C>T MANE Select NP_001785.2:n.170-211858C>T
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