Canonical Allele Identifier: CA2373783943
Gene: CDH4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61531684T= , CM000682.2:g.61531684T= GRCh38
NC_000020.10:g.60106740T= , CM000682.1:g.60106740T= GRCh37
NC_000020.9:g.59540135T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000614565.5:c.170-211879T= MANE Select ENSP00000484928.1:n.170-211879T=
ENST00000614565.4:c.170-211879T= ENSP00000484928.1:n.170-211879T=
NM_001252338.2:c.58+32192T= NP_001239267.1:n.58+32192T=
NM_001794.4:c.170-211879T= NP_001785.2:n.170-211879T=
NM_001794.5:c.170-211879T= MANE Select NP_001785.2:n.170-211879T=
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