Canonical Allele Identifier: CA2373989213
Gene: CDH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61928229A= , CM000682.2:g.61928229A= GRCh38
NC_000020.10:g.60503287A= , CM000682.1:g.60503287A= GRCh37
NC_000020.9:g.59936682A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.1811A= MANE Select ENSP00000484928.1:p.Tyr604=
ENST00000543233.2:c.1589A= ENSP00000443301.1:p.Tyr530=
ENST00000611855.4:c.1529A= ENSP00000480844.1:p.Tyr510=
ENST00000614565.4:c.1811A= ENSP00000484928.1:p.Tyr604=
NM_001252338.2:c.1700A= NP_001239267.1:p.Tyr567=
NM_001252339.2:c.1589A= NP_001239268.1:p.Tyr530=
NM_001794.4:c.1811A= NP_001785.2:p.Tyr604=
NM_001794.5:c.1811A= MANE Select NP_001785.2:p.Tyr604=
NM_001252339.3:c.1589A= NP_001239268.1:p.Tyr530=