Canonical Allele Identifier: CA1911368119
Gene: PCDH15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.55031224T= , CM000672.2:g.55031224T= GRCh38
NC_000010.10:g.56790984T= , CM000672.1:g.56790984T= GRCh37
NC_000010.9:g.56460990T= NCBI36
NG_009191.3:g.602959A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000458638.1:c.-79-133724A= ENSP00000394465.1:n.-79-133724A=
ENST00000613346.4:c.-79-133724A= ENSP00000481211.1:n.-79-133724A=
NM_001354404.1:c.-79-133724A= NP_001341333.1:n.-79-133724A=
XM_017016573.2:c.-156-82623A= XP_016872062.1:n.-156-82623A=
NM_001354404.2:c.-79-133724A= NP_001341333.1:n.-79-133724A=