Canonical Allele Identifier: CA317137186

Gene: CDH4

Linked Data

• dbSNP Id: rs903466552
• gnomAD v3: 20-61928083-C-G
• gnomAD v4: 20-61928083-C-G
• MyVariant Identifiers: chr20:g.60503141C>G (hg19) ; chr20:g.61928083C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61928083C>G , CM000682.2:g.61928083C>G	GRCh38
NC_000020.10:g.60503141C>G , CM000682.1:g.60503141C>G	GRCh37
NC_000020.9:g.59936536C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.1772-107C>G MANE Select	ENSP00000484928.1:n.1772-107C>G
ENST00000543233.2:c.1550-107C>G	ENSP00000443301.1:n.1550-107C>G
ENST00000611855.4:c.1490-107C>G	ENSP00000480844.1:n.1490-107C>G
ENST00000614565.4:c.1772-107C>G	ENSP00000484928.1:n.1772-107C>G
NM_001252338.2:c.1661-107C>G	NP_001239267.1:n.1661-107C>G
NM_001252339.2:c.1550-107C>G	NP_001239268.1:n.1550-107C>G
NM_001794.4:c.1772-107C>G	NP_001785.2:n.1772-107C>G
NM_001794.5:c.1772-107C>G MANE Select	NP_001785.2:n.1772-107C>G
NM_001252339.3:c.1550-107C>G	NP_001239268.1:n.1550-107C>G