Canonical Allele Identifier: CA511321932

Gene: CDH4

Linked Data

• MyVariant Identifiers: chr20:g.60503252A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61928194A>T , CM000682.2:g.61928194A>T	GRCh38
NC_000020.10:g.60503252A>T , CM000682.1:g.60503252A>T	GRCh37
NC_000020.9:g.59936647A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.1776A>T MANE Select	ENSP00000484928.1:p.Ile592=
ENST00000543233.2:c.1554A>T	ENSP00000443301.1:p.Ile518=
ENST00000611855.4:c.1494A>T	ENSP00000480844.1:p.Ile498=
ENST00000614565.4:c.1776A>T	ENSP00000484928.1:p.Ile592=
NM_001252338.2:c.1665A>T	NP_001239267.1:p.Ile555=
NM_001252339.2:c.1554A>T	NP_001239268.1:p.Ile518=
NM_001794.4:c.1776A>T	NP_001785.2:p.Ile592=
NM_001794.5:c.1776A>T MANE Select	NP_001785.2:p.Ile592=
NM_001252339.3:c.1554A>T	NP_001239268.1:p.Ile518=