Canonical Allele Identifier: CA2373784099
Gene: CDH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61532025T= , CM000682.2:g.61532025T= GRCh38
NC_000020.10:g.60107081T= , CM000682.1:g.60107081T= GRCh37
NC_000020.9:g.59540476T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.170-211538T= MANE Select ENSP00000484928.1:n.170-211538T=
ENST00000614565.4:c.170-211538T= ENSP00000484928.1:n.170-211538T=
NM_001252338.2:c.58+32533T= NP_001239267.1:n.58+32533T=
NM_001794.4:c.170-211538T= NP_001785.2:n.170-211538T=
NM_001794.5:c.170-211538T= MANE Select NP_001785.2:n.170-211538T=