Canonical Allele Identifier: CA2373989207
Gene: CDH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61928216A= , CM000682.2:g.61928216A= GRCh38
NC_000020.10:g.60503274A= , CM000682.1:g.60503274A= GRCh37
NC_000020.9:g.59936669A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.1798A= MANE Select ENSP00000484928.1:p.Thr600=
ENST00000543233.2:c.1576A= ENSP00000443301.1:p.Thr526=
ENST00000611855.4:c.1516A= ENSP00000480844.1:p.Thr506=
ENST00000614565.4:c.1798A= ENSP00000484928.1:p.Thr600=
NM_001252338.2:c.1687A= NP_001239267.1:p.Thr563=
NM_001252339.2:c.1576A= NP_001239268.1:p.Thr526=
NM_001794.4:c.1798A= NP_001785.2:p.Thr600=
NM_001794.5:c.1798A= MANE Select NP_001785.2:p.Thr600=
NM_001252339.3:c.1576A= NP_001239268.1:p.Thr526=