Canonical Allele Identifier: CA317411486
Gene: CDH4 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs116896199

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61531817A>G , CM000682.2:g.61531817A>G GRCh38
NC_000020.10:g.60106873A>G , CM000682.1:g.60106873A>G GRCh37
NC_000020.9:g.59540268A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001252338.2:c.58+32325A>G VV NP_001239267.1:p.=
NM_001794.4:c.170-211746A>G VV NP_001785.2:p.=
NM_001794.5:c.170-211746A>G VV MANE Preferred NP_001785.2:p.=
ENST00000614565.4:c.170-211746A>G ENSP00000484928.1:p.=