Canonical Allele Identifier: CA2373784066
Gene: CDH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61531952T= , CM000682.2:g.61531952T= GRCh38
NC_000020.10:g.60107008T= , CM000682.1:g.60107008T= GRCh37
NC_000020.9:g.59540403T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.170-211611T= MANE Select ENSP00000484928.1:n.170-211611T=
ENST00000614565.4:c.170-211611T= ENSP00000484928.1:n.170-211611T=
NM_001252338.2:c.58+32460T= NP_001239267.1:n.58+32460T=
NM_001794.4:c.170-211611T= NP_001785.2:n.170-211611T=
NM_001794.5:c.170-211611T= MANE Select NP_001785.2:n.170-211611T=