Canonical Allele Identifier: CA511322283

Gene: CDH4

Linked Data

• MyVariant Identifiers: chr20:g.60503447C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61928389C>A , CM000682.2:g.61928389C>A	GRCh38
NC_000020.10:g.60503447C>A , CM000682.1:g.60503447C>A	GRCh37
NC_000020.9:g.59936842C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.1971C>A MANE Select	ENSP00000484928.1:p.Ala657=
ENST00000543233.2:c.1749C>A	ENSP00000443301.1:p.Ala583=
ENST00000611855.4:c.1689C>A	ENSP00000480844.1:p.Ala563=
ENST00000614565.4:c.1971C>A	ENSP00000484928.1:p.Ala657=
NM_001252338.2:c.1860C>A	NP_001239267.1:p.Ala620=
NM_001252339.2:c.1749C>A	NP_001239268.1:p.Ala583=
NM_001794.4:c.1971C>A	NP_001785.2:p.Ala657=
NM_001794.5:c.1971C>A MANE Select	NP_001785.2:p.Ala657=
NM_001252339.3:c.1749C>A	NP_001239268.1:p.Ala583=