Canonical Allele Identifier: CA2373783999
Gene: CDH4 HGNC NCBI

Linked Data

dbSNP Id: rs2085956619

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61531779C>G , CM000682.2:g.61531779C>G GRCh38
NC_000020.10:g.60106835C>G , CM000682.1:g.60106835C>G GRCh37
NC_000020.9:g.59540230C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000614565.5:c.170-211784C>G MANE Select ENSP00000484928.1:n.170-211784C>G
ENST00000614565.4:c.170-211784C>G ENSP00000484928.1:n.170-211784C>G
NM_001252338.2:c.58+32287C>G NP_001239267.1:n.58+32287C>G
NM_001794.4:c.170-211784C>G NP_001785.2:n.170-211784C>G
NM_001794.5:c.170-211784C>G MANE Select NP_001785.2:n.170-211784C>G