Canonical Allele Identifier: CA511322190
Gene: CDH4 HGNC NCBI

Linked Data

dbSNP Id: rs1255039935
gnomAD v2: 20-60503351-G-A
gnomAD v3: 20-61928293-G-A
gnomAD v4: 20-61928293-G-A
MyVariant Identifiers: chr20:g.60503351G>A (hg19) chr20:g.61928293G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61928293G>A , CM000682.2:g.61928293G>A GRCh38
NC_000020.10:g.60503351G>A , CM000682.1:g.60503351G>A GRCh37
NC_000020.9:g.59936746G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.1875G>A MANE Select ENSP00000484928.1:p.Lys625=
ENST00000543233.2:c.1653G>A ENSP00000443301.1:p.Lys551=
ENST00000611855.4:c.1593G>A ENSP00000480844.1:p.Lys531=
ENST00000614565.4:c.1875G>A ENSP00000484928.1:p.Lys625=
NM_001252338.2:c.1764G>A NP_001239267.1:p.Lys588=
NM_001252339.2:c.1653G>A NP_001239268.1:p.Lys551=
NM_001794.4:c.1875G>A NP_001785.2:p.Lys625=
NM_001794.5:c.1875G>A MANE Select NP_001785.2:p.Lys625=
NM_001252339.3:c.1653G>A NP_001239268.1:p.Lys551=
Search 100 bp 5'
Search 100 bp 3'