Canonical Allele Identifier: CA2373989193
Gene: CDH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61928193T= , CM000682.2:g.61928193T= GRCh38
NC_000020.10:g.60503251T= , CM000682.1:g.60503251T= GRCh37
NC_000020.9:g.59936646T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.1775T= MANE Select ENSP00000484928.1:p.Ile592=
ENST00000543233.2:c.1553T= ENSP00000443301.1:p.Ile518=
ENST00000611855.4:c.1493T= ENSP00000480844.1:p.Ile498=
ENST00000614565.4:c.1775T= ENSP00000484928.1:p.Ile592=
NM_001252338.2:c.1664T= NP_001239267.1:p.Ile555=
NM_001252339.2:c.1553T= NP_001239268.1:p.Ile518=
NM_001794.4:c.1775T= NP_001785.2:p.Ile592=
NM_001794.5:c.1775T= MANE Select NP_001785.2:p.Ile592=
NM_001252339.3:c.1553T= NP_001239268.1:p.Ile518=