Canonical Allele Identifier: CA9934876
Gene: CDH4 HGNC NCBI

Linked Data

dbSNP Id: rs777402708
ExAC: 20:60503271 G / A
gnomAD v2: 20-60503271-G-A
gnomAD v3: 20-61928213-G-A
gnomAD v4: 20-61928213-G-A
MyVariant Identifiers: chr20:g.60503271G>A (hg19) chr20:g.61928213G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61928213G>A , CM000682.2:g.61928213G>A GRCh38
NC_000020.10:g.60503271G>A , CM000682.1:g.60503271G>A GRCh37
NC_000020.9:g.59936666G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.1795G>A MANE Select ENSP00000484928.1:p.Gly599Arg
ENST00000543233.2:c.1573G>A ENSP00000443301.1:p.Gly525Arg
ENST00000611855.4:c.1513G>A ENSP00000480844.1:p.Gly505Arg
ENST00000614565.4:c.1795G>A ENSP00000484928.1:p.Gly599Arg
NM_001252338.2:c.1684G>A NP_001239267.1:p.Gly562Arg
NM_001252339.2:c.1573G>A NP_001239268.1:p.Gly525Arg
NM_001794.4:c.1795G>A NP_001785.2:p.Gly599Arg
NM_001794.5:c.1795G>A MANE Select NP_001785.2:p.Gly599Arg
NM_001252339.3:c.1573G>A NP_001239268.1:p.Gly525Arg
Search 100 bp 5'
Search 100 bp 3'