Canonical Allele Identifier: CA2816926576
Gene: CDH4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61531765A>T , CM000682.2:g.61531765A>T GRCh38
NC_000020.10:g.60106821A>T , CM000682.1:g.60106821A>T GRCh37
NC_000020.9:g.59540216A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000614565.5:c.170-211798A>T MANE Select ENSP00000484928.1:n.170-211798A>T
ENST00000614565.4:c.170-211798A>T ENSP00000484928.1:n.170-211798A>T
NM_001252338.2:c.58+32273A>T NP_001239267.1:n.58+32273A>T
NM_001794.4:c.170-211798A>T NP_001785.2:n.170-211798A>T
NM_001794.5:c.170-211798A>T MANE Select NP_001785.2:n.170-211798A>T
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