Canonical Allele Identifier: CA1019134438
Gene: CDH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61928144_61928147del , CM000682.2:g.61928144_61928147del GRCh38
NC_000020.10:g.60503202_60503205del , CM000682.1:g.60503202_60503205del GRCh37
NC_000020.9:g.59936597_59936600del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.1772-46_1772-43del MANE Select ENSP00000484928.1:n.1772-46_1772-43del
ENST00000543233.2:c.1550-46_1550-43del ENSP00000443301.1:n.1550-46_1550-43del
ENST00000611855.4:c.1490-46_1490-43del ENSP00000480844.1:n.1490-46_1490-43del
ENST00000614565.4:c.1772-46_1772-43del ENSP00000484928.1:n.1772-46_1772-43del
NM_001252338.2:c.1661-46_1661-43del NP_001239267.1:n.1661-46_1661-43del
NM_001252339.2:c.1550-46_1550-43del NP_001239268.1:n.1550-46_1550-43del
NM_001794.4:c.1772-46_1772-43del NP_001785.2:n.1772-46_1772-43del
NM_001794.5:c.1772-46_1772-43del MANE Select NP_001785.2:n.1772-46_1772-43del
NM_001252339.3:c.1550-46_1550-43del NP_001239268.1:n.1550-46_1550-43del