Canonical Allele Identifier: CA2373838813
Community Standard Title: NM_001794.5(CDH4):c.170-106125C=
Gene: CDH4 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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