Canonical Allele Identifier: CA1911368136
Gene: PCDH15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.55031258G= , CM000672.2:g.55031258G= GRCh38
NC_000010.10:g.56791018G= , CM000672.1:g.56791018G= GRCh37
NC_000010.9:g.56461024G= NCBI36
NG_009191.3:g.602925C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000458638.1:c.-79-133758C= ENSP00000394465.1:n.-79-133758C=
ENST00000613346.4:c.-79-133758C= ENSP00000481211.1:n.-79-133758C=
NM_001354404.1:c.-79-133758C= NP_001341333.1:n.-79-133758C=
XM_017016573.2:c.-156-82657C= XP_016872062.1:n.-156-82657C=
NM_001354404.2:c.-79-133758C= NP_001341333.1:n.-79-133758C=