Canonical Allele Identifier: CA2373989174
Gene: CDH4 HGNC NCBI

Linked Data

dbSNP Id: rs2055065396

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61928168_61928170del , CM000682.2:g.61928168_61928170del GRCh38
NC_000020.10:g.60503226_60503228del , CM000682.1:g.60503226_60503228del GRCh37
NC_000020.9:g.59936621_59936623del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.1772-22_1772-20del MANE Select ENSP00000484928.1:n.1772-22_1772-20del
ENST00000543233.2:c.1550-22_1550-20del ENSP00000443301.1:n.1550-22_1550-20del
ENST00000611855.4:c.1490-22_1490-20del ENSP00000480844.1:n.1490-22_1490-20del
ENST00000614565.4:c.1772-22_1772-20del ENSP00000484928.1:n.1772-22_1772-20del
NM_001252338.2:c.1661-22_1661-20del NP_001239267.1:n.1661-22_1661-20del
NM_001252339.2:c.1550-22_1550-20del NP_001239268.1:n.1550-22_1550-20del
NM_001794.4:c.1772-22_1772-20del NP_001785.2:n.1772-22_1772-20del
NM_001794.5:c.1772-22_1772-20del MANE Select NP_001785.2:n.1772-22_1772-20del
NM_001252339.3:c.1550-22_1550-20del NP_001239268.1:n.1550-22_1550-20del