Canonical Allele Identifier: CA409508630

Gene: CDH4

Linked Data

• gnomAD v4: 20-61928211-C-T
• MyVariant Identifiers: chr20:g.60503269C>T (hg19) ; chr20:g.61928211C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.1793C>T MANE Select	ENSP00000484928.1:p.Thr598Ile
ENST00000543233.2:c.1571C>T	ENSP00000443301.1:p.Thr524Ile
ENST00000611855.4:c.1511C>T	ENSP00000480844.1:p.Thr504Ile
ENST00000614565.4:c.1793C>T	ENSP00000484928.1:p.Thr598Ile
NM_001252338.2:c.1682C>T	NP_001239267.1:p.Thr561Ile
NM_001252339.2:c.1571C>T	NP_001239268.1:p.Thr524Ile
NM_001794.4:c.1793C>T	NP_001785.2:p.Thr598Ile
NM_001794.5:c.1793C>T MANE Select	NP_001785.2:p.Thr598Ile
NM_001252339.3:c.1571C>T	NP_001239268.1:p.Thr524Ile