Canonical Allele Identifier: CA409508777

Gene: CDH4

Linked Data

• MyVariant Identifiers: chr20:g.60503302A>T (hg19) ; chr20:g.61928244A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61928244A>T , CM000682.2:g.61928244A>T	GRCh38
NC_000020.10:g.60503302A>T , CM000682.1:g.60503302A>T	GRCh37
NC_000020.9:g.59936697A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.1826A>T MANE Select	ENSP00000484928.1:p.Asn609Ile
ENST00000543233.2:c.1604A>T	ENSP00000443301.1:p.Asn535Ile
ENST00000611855.4:c.1544A>T	ENSP00000480844.1:p.Asn515Ile
ENST00000614565.4:c.1826A>T	ENSP00000484928.1:p.Asn609Ile
NM_001252338.2:c.1715A>T	NP_001239267.1:p.Asn572Ile
NM_001252339.2:c.1604A>T	NP_001239268.1:p.Asn535Ile
NM_001794.4:c.1826A>T	NP_001785.2:p.Asn609Ile
NM_001794.5:c.1826A>T MANE Select	NP_001785.2:p.Asn609Ile
NM_001252339.3:c.1604A>T	NP_001239268.1:p.Asn535Ile