Canonical Allele Identifier: CA2373989125

Gene: CDH4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61928082_61928084delinsCCT , CM000682.2:g.61928082_61928084delinsCCT	GRCh38
NC_000020.10:g.60503140_60503142delinsCCT , CM000682.1:g.60503140_60503142delinsCCT	GRCh37
NC_000020.9:g.59936535_59936537delinsCCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.1772-108_1772-106delinsCCT MANE Select	ENSP00000484928.1:n.1772-108_1772-106delinsCCT
ENST00000543233.2:c.1550-108_1550-106delinsCCT	ENSP00000443301.1:n.1550-108_1550-106delinsCCT
ENST00000611855.4:c.1490-108_1490-106delinsCCT	ENSP00000480844.1:n.1490-108_1490-106delinsCCT
ENST00000614565.4:c.1772-108_1772-106delinsCCT	ENSP00000484928.1:n.1772-108_1772-106delinsCCT
NM_001252338.2:c.1661-108_1661-106delinsCCT	NP_001239267.1:n.1661-108_1661-106delinsCCT
NM_001252339.2:c.1550-108_1550-106delinsCCT	NP_001239268.1:n.1550-108_1550-106delinsCCT
NM_001794.4:c.1772-108_1772-106delinsCCT	NP_001785.2:n.1772-108_1772-106delinsCCT
NM_001794.5:c.1772-108_1772-106delinsCCT MANE Select	NP_001785.2:n.1772-108_1772-106delinsCCT
NM_001252339.3:c.1550-108_1550-106delinsCCT	NP_001239268.1:n.1550-108_1550-106delinsCCT