Canonical Allele Identifier: CA2373927461
Community Standard Title: NM_001794.5(CDH4):c.576+33561G=
Gene: CDH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61806743G= , CM000682.2:g.61806743G= GRCh38
NC_000020.10:g.60381799G= , CM000682.1:g.60381799G= GRCh37
NC_000020.9:g.59815194G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001794.5:c.576+33561G= MANE Select NP_001785.2:n.576+33561G=
ENST00000614565.5:c.576+33561G= MANE Select ENSP00000484928.1:n.576+33561G=
NM_001252338.2:c.465+33561G= NP_001239267.1:n.465+33561G=
NM_001252339.2:c.354+33561G= NP_001239268.1:n.354+33561G=
NM_001252339.3:c.354+33561G= NP_001239268.1:n.354+33561G=
NM_001794.4:c.576+33561G= NP_001785.2:n.576+33561G=
ENST00000543233.2:c.354+33561G= ENSP00000443301.1:n.354+33561G=
ENST00000611855.4:c.294+33561G= ENSP00000480844.1:n.294+33561G=
ENST00000614565.4:c.576+33561G= ENSP00000484928.1:n.576+33561G=