Canonical Allele Identifier: CA9934878

Gene: CDH4

Linked Data

• dbSNP Id: rs111983852
• ExAC: 20:60503273 G / T
• gnomAD v2: 20-60503273-G-T
• gnomAD v4: 20-61928215-G-T
• MyVariant Identifiers: chr20:g.60503273G>T (hg19) ; chr20:g.61928215G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61928215G>T , CM000682.2:g.61928215G>T	GRCh38
NC_000020.10:g.60503273G>T , CM000682.1:g.60503273G>T	GRCh37
NC_000020.9:g.59936668G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.1797G>T MANE Select	ENSP00000484928.1:p.Gly599=
ENST00000543233.2:c.1575G>T	ENSP00000443301.1:p.Gly525=
ENST00000611855.4:c.1515G>T	ENSP00000480844.1:p.Gly505=
ENST00000614565.4:c.1797G>T	ENSP00000484928.1:p.Gly599=
NM_001252338.2:c.1686G>T	NP_001239267.1:p.Gly562=
NM_001252339.2:c.1575G>T	NP_001239268.1:p.Gly525=
NM_001794.4:c.1797G>T	NP_001785.2:p.Gly599=
NM_001794.5:c.1797G>T MANE Select	NP_001785.2:p.Gly599=
NM_001252339.3:c.1575G>T	NP_001239268.1:p.Gly525=