Canonical Allele Identifier: CA409508878

Gene: CDH4

Linked Data

• gnomAD v4: 20-61928268-C-G
• MyVariant Identifiers: chr20:g.60503326C>G (hg19) ; chr20:g.61928268C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61928268C>G , CM000682.2:g.61928268C>G	GRCh38
NC_000020.10:g.60503326C>G , CM000682.1:g.60503326C>G	GRCh37
NC_000020.9:g.59936721C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.1850C>G MANE Select	ENSP00000484928.1:p.Pro617Arg
ENST00000543233.2:c.1628C>G	ENSP00000443301.1:p.Pro543Arg
ENST00000611855.4:c.1568C>G	ENSP00000480844.1:p.Pro523Arg
ENST00000614565.4:c.1850C>G	ENSP00000484928.1:p.Pro617Arg
NM_001252338.2:c.1739C>G	NP_001239267.1:p.Pro580Arg
NM_001252339.2:c.1628C>G	NP_001239268.1:p.Pro543Arg
NM_001794.4:c.1850C>G	NP_001785.2:p.Pro617Arg
NM_001794.5:c.1850C>G MANE Select	NP_001785.2:p.Pro617Arg
NM_001252339.3:c.1628C>G	NP_001239268.1:p.Pro543Arg