Canonical Allele Identifier: CA317137183

Gene: CDH4

Linked Data

• dbSNP Id: rs146291224
• gnomAD v2: 20-60503132-CAT-C
• gnomAD v3: 20-61928074-CAT-C
• gnomAD v4: 20-61928074-CAT-C
• MyVariant Identifiers: chr20:g.60503133_60503134del (hg19) ; chr20:g.61928075_61928076del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61928075_61928076del , CM000682.2:g.61928075_61928076del	GRCh38
NC_000020.10:g.60503133_60503134del , CM000682.1:g.60503133_60503134del	GRCh37
NC_000020.9:g.59936528_59936529del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.1772-115_1772-114del MANE Select	ENSP00000484928.1:n.1772-115_1772-114del
ENST00000543233.2:c.1550-115_1550-114del	ENSP00000443301.1:n.1550-115_1550-114del
ENST00000611855.4:c.1490-115_1490-114del	ENSP00000480844.1:n.1490-115_1490-114del
ENST00000614565.4:c.1772-115_1772-114del	ENSP00000484928.1:n.1772-115_1772-114del
NM_001252338.2:c.1661-115_1661-114del	NP_001239267.1:n.1661-115_1661-114del
NM_001252339.2:c.1550-115_1550-114del	NP_001239268.1:n.1550-115_1550-114del
NM_001794.4:c.1772-115_1772-114del	NP_001785.2:n.1772-115_1772-114del
NM_001794.5:c.1772-115_1772-114del MANE Select	NP_001785.2:n.1772-115_1772-114del
NM_001252339.3:c.1550-115_1550-114del	NP_001239268.1:n.1550-115_1550-114del