Canonical Allele Identifier: CA636608665
Gene: CDH4 HGNC NCBI

Linked Data

dbSNP Id: rs1389913690
gnomAD v2: 20-60503203-G-A
gnomAD v4: 20-61928145-G-A
MyVariant Identifiers: chr20:g.60503203G>A (hg19) chr20:g.61928145G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61928145G>A , CM000682.2:g.61928145G>A GRCh38
NC_000020.10:g.60503203G>A , CM000682.1:g.60503203G>A GRCh37
NC_000020.9:g.59936598G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.1772-45G>A MANE Select ENSP00000484928.1:n.1772-45G>A
ENST00000543233.2:c.1550-45G>A ENSP00000443301.1:n.1550-45G>A
ENST00000611855.4:c.1490-45G>A ENSP00000480844.1:n.1490-45G>A
ENST00000614565.4:c.1772-45G>A ENSP00000484928.1:n.1772-45G>A
NM_001252338.2:c.1661-45G>A NP_001239267.1:n.1661-45G>A
NM_001252339.2:c.1550-45G>A NP_001239268.1:n.1550-45G>A
NM_001794.4:c.1772-45G>A NP_001785.2:n.1772-45G>A
NM_001794.5:c.1772-45G>A MANE Select NP_001785.2:n.1772-45G>A
NM_001252339.3:c.1550-45G>A NP_001239268.1:n.1550-45G>A
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