Canonical Allele Identifier: CA2816926579
Gene: CDH4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61531991G>C , CM000682.2:g.61531991G>C GRCh38
NC_000020.10:g.60107047G>C , CM000682.1:g.60107047G>C GRCh37
NC_000020.9:g.59540442G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.170-211572G>C MANE Select ENSP00000484928.1:n.170-211572G>C
ENST00000614565.4:c.170-211572G>C ENSP00000484928.1:n.170-211572G>C
NM_001252338.2:c.58+32499G>C NP_001239267.1:n.58+32499G>C
NM_001794.4:c.170-211572G>C NP_001785.2:n.170-211572G>C
NM_001794.5:c.170-211572G>C MANE Select NP_001785.2:n.170-211572G>C
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