Canonical Allele Identifier: CA409508689
Gene: CDH4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61928226T>A , CM000682.2:g.61928226T>A GRCh38
NC_000020.10:g.60503284T>A , CM000682.1:g.60503284T>A GRCh37
NC_000020.9:g.59936679T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.1808T>A MANE Select ENSP00000484928.1:p.Ile603Asn
ENST00000543233.2:c.1586T>A ENSP00000443301.1:p.Ile529Asn
ENST00000611855.4:c.1526T>A ENSP00000480844.1:p.Ile509Asn
ENST00000614565.4:c.1808T>A ENSP00000484928.1:p.Ile603Asn
NM_001252338.2:c.1697T>A NP_001239267.1:p.Ile566Asn
NM_001252339.2:c.1586T>A NP_001239268.1:p.Ile529Asn
NM_001794.4:c.1808T>A NP_001785.2:p.Ile603Asn
NM_001794.5:c.1808T>A MANE Select NP_001785.2:p.Ile603Asn
NM_001252339.3:c.1586T>A NP_001239268.1:p.Ile529Asn