Canonical Allele Identifier: CA2653589326

Gene: CDH4

Linked Data

• gnomAD v4: 20-61928173-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61928177_61928178del , CM000682.2:g.61928177_61928178del	GRCh38
NC_000020.10:g.60503235_60503236del , CM000682.1:g.60503235_60503236del	GRCh37
NC_000020.9:g.59936630_59936631del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.1772-13_1772-12del MANE Select	ENSP00000484928.1:n.1772-13_1772-12del
ENST00000543233.2:c.1550-13_1550-12del	ENSP00000443301.1:n.1550-13_1550-12del
ENST00000611855.4:c.1490-13_1490-12del	ENSP00000480844.1:n.1490-13_1490-12del
ENST00000614565.4:c.1772-13_1772-12del	ENSP00000484928.1:n.1772-13_1772-12del
NM_001252338.2:c.1661-13_1661-12del	NP_001239267.1:n.1661-13_1661-12del
NM_001252339.2:c.1550-13_1550-12del	NP_001239268.1:n.1550-13_1550-12del
NM_001794.4:c.1772-13_1772-12del	NP_001785.2:n.1772-13_1772-12del
NM_001794.5:c.1772-13_1772-12del MANE Select	NP_001785.2:n.1772-13_1772-12del
NM_001252339.3:c.1550-13_1550-12del	NP_001239268.1:n.1550-13_1550-12del