Canonical Allele Identifier: CA2653589342

Gene: CDH4

Linked Data

• gnomAD v4: 20-61928269-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61928271del , CM000682.2:g.61928271del	GRCh38
NC_000020.10:g.60503329del , CM000682.1:g.60503329del	GRCh37
NC_000020.9:g.59936724del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.1853del MANE Select	ENSP00000484928.1:p.Lys618ArgfsTer11
ENST00000543233.2:c.1631del	ENSP00000443301.1:p.Lys544ArgfsTer11
ENST00000611855.4:c.1571del	ENSP00000480844.1:p.Lys524ArgfsTer11
ENST00000614565.4:c.1853del	ENSP00000484928.1:p.Lys618ArgfsTer11
NM_001252338.2:c.1742del	NP_001239267.1:p.Lys581ArgfsTer11
NM_001252339.2:c.1631del	NP_001239268.1:p.Lys544ArgfsTer11
NM_001794.4:c.1853del	NP_001785.2:p.Lys618ArgfsTer11
NM_001794.5:c.1853del MANE Select	NP_001785.2:p.Lys618ArgfsTer11
NM_001252339.3:c.1631del	NP_001239268.1:p.Lys544ArgfsTer11