Canonical Allele Identifier: CA666578655
Gene: PCDH15 HGNC NCBI

Linked Data

dbSNP Id: rs1188930817

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.55089132del , CM000672.2:g.55089132del GRCh38
NC_000010.10:g.56848892del , CM000672.1:g.56848892del GRCh37
NC_000010.9:g.56518898del NCBI36
NG_009191.3:g.545055del

Transcript Alleles

HGVS Amino-acid change
ENST00000458638.1:c.-80+77448del ENSP00000394465.1:n.-80+77448del
ENST00000613346.4:c.-80+77448del ENSP00000481211.1:n.-80+77448del
NM_001354404.1:c.-80+77448del NP_001341333.1:n.-80+77448del
XM_017016573.2:c.-157+77448del XP_016872062.1:n.-157+77448del
NM_001354404.2:c.-80+77448del NP_001341333.1:n.-80+77448del