Canonical Allele Identifier: CA2373989141
Gene: CDH4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61928111T= , CM000682.2:g.61928111T= GRCh38
NC_000020.10:g.60503169T= , CM000682.1:g.60503169T= GRCh37
NC_000020.9:g.59936564T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.1772-79T= MANE Select ENSP00000484928.1:n.1772-79T=
ENST00000543233.2:c.1550-79T= ENSP00000443301.1:n.1550-79T=
ENST00000611855.4:c.1490-79T= ENSP00000480844.1:n.1490-79T=
ENST00000614565.4:c.1772-79T= ENSP00000484928.1:n.1772-79T=
NM_001252338.2:c.1661-79T= NP_001239267.1:n.1661-79T=
NM_001252339.2:c.1550-79T= NP_001239268.1:n.1550-79T=
NM_001794.4:c.1772-79T= NP_001785.2:n.1772-79T=
NM_001794.5:c.1772-79T= MANE Select NP_001785.2:n.1772-79T=
NM_001252339.3:c.1550-79T= NP_001239268.1:n.1550-79T=
Search 100 bp 5'
Search 100 bp 3'