Canonical Allele Identifier: CA1911368116
Gene: PCDH15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.55031216C= , CM000672.2:g.55031216C= GRCh38
NC_000010.10:g.56790976C= , CM000672.1:g.56790976C= GRCh37
NC_000010.9:g.56460982C= NCBI36
NG_009191.3:g.602967G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000458638.1:c.-79-133716G= ENSP00000394465.1:n.-79-133716G=
ENST00000613346.4:c.-79-133716G= ENSP00000481211.1:n.-79-133716G=
NM_001354404.1:c.-79-133716G= NP_001341333.1:n.-79-133716G=
XM_017016573.2:c.-156-82615G= XP_016872062.1:n.-156-82615G=
NM_001354404.2:c.-79-133716G= NP_001341333.1:n.-79-133716G=