Canonical Allele Identifier: CA2373989242
Gene: CDH4 HGNC NCBI

Linked Data

dbSNP Id: rs2055067688

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61928291_61928293del , CM000682.2:g.61928291_61928293del GRCh38
NC_000020.10:g.60503349_60503351del , CM000682.1:g.60503349_60503351del GRCh37
NC_000020.9:g.59936744_59936746del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.1873_1875del MANE Select ENSP00000484928.1:p.Lys625del
ENST00000543233.2:c.1651_1653del ENSP00000443301.1:p.Lys551del
ENST00000611855.4:c.1591_1593del ENSP00000480844.1:p.Lys531del
ENST00000614565.4:c.1873_1875del ENSP00000484928.1:p.Lys625del
NM_001252338.2:c.1762_1764del NP_001239267.1:p.Lys588del
NM_001252339.2:c.1651_1653del NP_001239268.1:p.Lys551del
NM_001794.4:c.1873_1875del NP_001785.2:p.Lys625del
NM_001794.5:c.1873_1875del MANE Select NP_001785.2:p.Lys625del
NM_001252339.3:c.1651_1653del NP_001239268.1:p.Lys551del