Canonical Allele Identifier: CA2373989238
Gene: CDH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61928285T= , CM000682.2:g.61928285T= GRCh38
NC_000020.10:g.60503343T= , CM000682.1:g.60503343T= GRCh37
NC_000020.9:g.59936738T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.1867T= MANE Select ENSP00000484928.1:p.Cys623=
ENST00000543233.2:c.1645T= ENSP00000443301.1:p.Cys549=
ENST00000611855.4:c.1585T= ENSP00000480844.1:p.Cys529=
ENST00000614565.4:c.1867T= ENSP00000484928.1:p.Cys623=
NM_001252338.2:c.1756T= NP_001239267.1:p.Cys586=
NM_001252339.2:c.1645T= NP_001239268.1:p.Cys549=
NM_001794.4:c.1867T= NP_001785.2:p.Cys623=
NM_001794.5:c.1867T= MANE Select NP_001785.2:p.Cys623=
NM_001252339.3:c.1645T= NP_001239268.1:p.Cys549=