Canonical Allele Identifier: CA409508705

Gene: CDH4

Linked Data

• MyVariant Identifiers: chr20:g.60503287A>G (hg19) ; chr20:g.61928229A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61928229A>G , CM000682.2:g.61928229A>G	GRCh38
NC_000020.10:g.60503287A>G , CM000682.1:g.60503287A>G	GRCh37
NC_000020.9:g.59936682A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.1811A>G MANE Select	ENSP00000484928.1:p.Tyr604Cys
ENST00000543233.2:c.1589A>G	ENSP00000443301.1:p.Tyr530Cys
ENST00000611855.4:c.1529A>G	ENSP00000480844.1:p.Tyr510Cys
ENST00000614565.4:c.1811A>G	ENSP00000484928.1:p.Tyr604Cys
NM_001252338.2:c.1700A>G	NP_001239267.1:p.Tyr567Cys
NM_001252339.2:c.1589A>G	NP_001239268.1:p.Tyr530Cys
NM_001794.4:c.1811A>G	NP_001785.2:p.Tyr604Cys
NM_001794.5:c.1811A>G MANE Select	NP_001785.2:p.Tyr604Cys
NM_001252339.3:c.1589A>G	NP_001239268.1:p.Tyr530Cys