Canonical Allele Identifier: CA15969052
Gene: CDH4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61683795G>A , CM000682.2:g.61683795G>A GRCh38
NC_000020.10:g.60258851G>A , CM000682.1:g.60258851G>A GRCh37
NC_000020.9:g.59692246G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.170-59768G>A MANE Select ENSP00000484928.1:n.170-59768G>A
ENST00000543233.2:c.-53-59768G>A ENSP00000443301.1:n.-53-59768G>A
ENST00000611855.4:c.50-59768G>A ENSP00000480844.1:n.50-59768G>A
ENST00000614565.4:c.170-59768G>A ENSP00000484928.1:n.170-59768G>A
NM_001252338.2:c.59-59768G>A NP_001239267.1:n.59-59768G>A
NM_001252339.2:c.-53-59768G>A NP_001239268.1:n.-53-59768G>A
NM_001794.4:c.170-59768G>A NP_001785.2:n.170-59768G>A
NM_001794.5:c.170-59768G>A MANE Select NP_001785.2:n.170-59768G>A
NM_001252339.3:c.-53-59768G>A NP_001239268.1:n.-53-59768G>A
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