Canonical Allele Identifier: CA409508627

Gene: CDH4

Linked Data

• MyVariant Identifiers: chr20:g.60503269C>A (hg19) ; chr20:g.61928211C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61928211C>A , CM000682.2:g.61928211C>A	GRCh38
NC_000020.10:g.60503269C>A , CM000682.1:g.60503269C>A	GRCh37
NC_000020.9:g.59936664C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.1793C>A MANE Select	ENSP00000484928.1:p.Thr598Asn
ENST00000543233.2:c.1571C>A	ENSP00000443301.1:p.Thr524Asn
ENST00000611855.4:c.1511C>A	ENSP00000480844.1:p.Thr504Asn
ENST00000614565.4:c.1793C>A	ENSP00000484928.1:p.Thr598Asn
NM_001252338.2:c.1682C>A	NP_001239267.1:p.Thr561Asn
NM_001252339.2:c.1571C>A	NP_001239268.1:p.Thr524Asn
NM_001794.4:c.1793C>A	NP_001785.2:p.Thr598Asn
NM_001794.5:c.1793C>A MANE Select	NP_001785.2:p.Thr598Asn
NM_001252339.3:c.1571C>A	NP_001239268.1:p.Thr524Asn