Canonical Allele Identifier: CA2569582544
Gene: PCDH15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.53806461_53806462del , CM000672.2:g.53806461_53806462del GRCh38
NC_000010.10:g.55566221_55566222del , CM000672.1:g.55566221_55566222del GRCh37
NC_000010.9:g.55236227_55236228del NCBI36
NG_009191.2:g.999831_999832del
NG_009191.3:g.1827722_1827723del

Transcript Alleles

HGVS Amino-acid Change
ENST00000642496.1:c.4200_4201del
ENST00000644397.2:c.*118_*119del MANE Select ENSP00000495195.1:n.*118_*119del
ENST00000373965.6:c.*118_*119del ENSP00000363076.3:n.*118_*119del
ENST00000414778.5:c.*118_*119del ENSP00000410304.2:n.*118_*119del
ENST00000495484.5:c.*118_*119del ENSP00000480780.1:n.*118_*119del
ENST00000614895.4:c.*118_*119del ENSP00000478512.1:n.*118_*119del
ENST00000616114.4:c.*118_*119del ENSP00000483745.1:n.*118_*119del
ENST00000621708.4:c.*118_*119del ENSP00000484454.1:n.*118_*119del
NM_001142771.1:c.*118_*119del NP_001136243.1:n.*118_*119del
NM_001142772.1:c.*118_*119del NP_001136244.1:n.*118_*119del
NM_001354420.1:c.*118_*119del NP_001341349.1:n.*118_*119del
NM_001354429.1:c.*118_*119del NP_001341358.1:n.*118_*119del
XR_001747192.2:n.11633_11634del
XR_001747193.2:n.11624_11625del
NM_001142771.2:c.*118_*119del NP_001136243.1:n.*118_*119del
NM_001142772.2:c.*118_*119del NP_001136244.1:n.*118_*119del
NM_001354420.2:c.*118_*119del NP_001341349.1:n.*118_*119del
NM_001354429.2:c.*118_*119del NP_001341358.1:n.*118_*119del
NM_001384140.1:c.*118_*119del MANE Select NP_001371069.1:n.*118_*119del