Canonical Allele Identifier: CA409509014

Gene: CDH4

Linked Data

• gnomAD v4: 20-61928297-A-G
• MyVariant Identifiers: chr20:g.60503355A>G (hg19) ; chr20:g.61928297A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61928297A>G , CM000682.2:g.61928297A>G	GRCh38
NC_000020.10:g.60503355A>G , CM000682.1:g.60503355A>G	GRCh37
NC_000020.9:g.59936750A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.1879A>G MANE Select	ENSP00000484928.1:p.Asn627Asp
ENST00000543233.2:c.1657A>G	ENSP00000443301.1:p.Asn553Asp
ENST00000611855.4:c.1597A>G	ENSP00000480844.1:p.Asn533Asp
ENST00000614565.4:c.1879A>G	ENSP00000484928.1:p.Asn627Asp
NM_001252338.2:c.1768A>G	NP_001239267.1:p.Asn590Asp
NM_001252339.2:c.1657A>G	NP_001239268.1:p.Asn553Asp
NM_001794.4:c.1879A>G	NP_001785.2:p.Asn627Asp
NM_001794.5:c.1879A>G MANE Select	NP_001785.2:p.Asn627Asp
NM_001252339.3:c.1657A>G	NP_001239268.1:p.Asn553Asp