Canonical Allele Identifier: CA9934907
Gene: CDH4 HGNC NCBI

Linked Data

dbSNP Id: rs143694141
ExAC: 20:60503397 G / A
gnomAD v2: 20-60503397-G-A
gnomAD v3: 20-61928339-G-A
gnomAD v4: 20-61928339-G-A
COSMIC: COSM2766006
MyVariant Identifiers: chr20:g.60503397G>A (hg19) chr20:g.61928339G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61928339G>A , CM000682.2:g.61928339G>A GRCh38
NC_000020.10:g.60503397G>A , CM000682.1:g.60503397G>A GRCh37
NC_000020.9:g.59936792G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.1921G>A MANE Select ENSP00000484928.1:p.Asp641Asn
ENST00000543233.2:c.1699G>A ENSP00000443301.1:p.Asp567Asn
ENST00000611855.4:c.1639G>A ENSP00000480844.1:p.Asp547Asn
ENST00000614565.4:c.1921G>A ENSP00000484928.1:p.Asp641Asn
NM_001252338.2:c.1810G>A NP_001239267.1:p.Asp604Asn
NM_001252339.2:c.1699G>A NP_001239268.1:p.Asp567Asn
NM_001794.4:c.1921G>A NP_001785.2:p.Asp641Asn
NM_001794.5:c.1921G>A MANE Select NP_001785.2:p.Asp641Asn
NM_001252339.3:c.1699G>A NP_001239268.1:p.Asp567Asn
Search 100 bp 5'
Search 100 bp 3'