Canonical Allele Identifier: CA511321961

Gene: CDH4

Linked Data

• MyVariant Identifiers: chr20:g.60503276C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61928218C>G , CM000682.2:g.61928218C>G	GRCh38
NC_000020.10:g.60503276C>G , CM000682.1:g.60503276C>G	GRCh37
NC_000020.9:g.59936671C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.1800C>G MANE Select	ENSP00000484928.1:p.Thr600=
ENST00000543233.2:c.1578C>G	ENSP00000443301.1:p.Thr526=
ENST00000611855.4:c.1518C>G	ENSP00000480844.1:p.Thr506=
ENST00000614565.4:c.1800C>G	ENSP00000484928.1:p.Thr600=
NM_001252338.2:c.1689C>G	NP_001239267.1:p.Thr563=
NM_001252339.2:c.1578C>G	NP_001239268.1:p.Thr526=
NM_001794.4:c.1800C>G	NP_001785.2:p.Thr600=
NM_001794.5:c.1800C>G MANE Select	NP_001785.2:p.Thr600=
NM_001252339.3:c.1578C>G	NP_001239268.1:p.Thr526=