Canonical Allele Identifier: CA16041357
Gene: PCDH15 HGNC NCBI

Linked Data

ClinVar Variation Id: 370252
ClinVar RCV Id: RCV000411267
dbSNP Id: rs1057516351

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.53827448del , CM000672.2:g.53827448del GRCh38
NC_000010.10:g.55587208del , CM000672.1:g.55587208del GRCh37
NC_000010.9:g.55257214del NCBI36
NG_009191.2:g.978845del
NG_009191.3:g.1806736del

Transcript Alleles

HGVS Amino-acid change
ENST00000613657.6:c.4349del ENSP00000482794.1:p.Pro1450ArgfsTer?
ENST00000320301.11:c.4313del MANE Plus Clinical ENSP00000322604.6:p.Pro1438ArgfsTer?
ENST00000395445.6:c.4334del ENSP00000378832.2:p.Pro1445ArgfsTer?
ENST00000613657.5:c.4349del ENSP00000482794.1:p.Pro1450ArgfsTer?
ENST00000642496.1:c.3172del
ENST00000644397.2:c.4313del MANE Select ENSP00000495195.1:p.Pro1438ArgfsTer30
ENST00000320301.10:c.4313del ENSP00000322604.6:p.Pro1438ArgfsTer?
ENST00000361849.7:c.4313del ENSP00000354950.3:p.Pro1438ArgfsTer?
ENST00000373956.7:c.*2268del ENSP00000363067.4:n.*2268del
ENST00000373957.7:c.4328del ENSP00000363068.4:p.Pro1443ArgfsTer?
ENST00000373965.6:c.4313del ENSP00000363076.3:p.Pro1438ArgfsTer?
ENST00000395430.5:c.4304del ENSP00000378818.1:p.Pro1435ArgfsTer?
ENST00000395432.6:c.4193del ENSP00000378820.2:p.Pro1398ArgfsTer?
ENST00000395433.5:c.4238del ENSP00000378821.1:p.Pro1413ArgfsTer?
ENST00000395438.5:c.4316del ENSP00000378826.2:p.Pro1439ArgfsTer19
ENST00000395440.5:c.1306-17901del ENSP00000378827.1:n.1306-17901del
ENST00000395442.5:c.1099-17901del ENSP00000378829.1:n.1099-17901del
ENST00000395445.5:c.4334del ENSP00000378832.2:p.Pro1445ArgfsTer?
ENST00000395446.5:c.2092-17901del ENSP00000378833.1:n.2092-17901del
ENST00000409834.5:c.3146del ENSP00000386693.1:p.Pro1049ArgfsTer29
ENST00000414367.5:c.*393del ENSP00000412531.1:n.*393del
ENST00000414778.5:c.4316del ENSP00000410304.2:p.Pro1439ArgfsTer?
ENST00000437009.5:c.4100del ENSP00000412628.2:p.Pro1367ArgfsTer?
ENST00000448885.5:c.*2268del ENSP00000412320.1:n.*2268del
ENST00000463095.2:n.1332del
ENST00000495484.5:c.461+3868del ENSP00000480780.1:n.461+3868del
ENST00000612394.4:c.4352del ENSP00000482921.1:p.Pro1451ArgfsTer?
ENST00000613657.4:c.4349del ENSP00000482794.1:p.Pro1450ArgfsTer?
ENST00000614895.4:c.4331del ENSP00000478512.1:p.Pro1444ArgfsTer?
ENST00000616114.4:c.4313del ENSP00000483745.1:p.Pro1438ArgfsTer?
ENST00000617051.4:c.4331del ENSP00000484703.1:p.Pro1444ArgfsTer?
ENST00000617271.4:c.4313del ENSP00000478076.1:p.Pro1438ArgfsTer29
ENST00000618301.4:c.539del ENSP00000482780.1:p.Pro180ArgfsTer19
ENST00000621708.4:c.4328del ENSP00000484454.1:p.Pro1443ArgfsTer?
ENST00000622048.4:c.4103del ENSP00000482329.1:p.Pro1368ArgfsTer?
NM_001142763.1:c.4328del NP_001136235.1:p.Pro1443ArgfsTer?
NM_001142764.1:c.4313del NP_001136236.1:p.Pro1438ArgfsTer?
NM_001142765.1:c.4100del NP_001136237.1:p.Pro1367ArgfsTer?
NM_001142766.1:c.4304del NP_001136238.1:p.Pro1435ArgfsTer?
NM_001142767.1:c.4193del NP_001136239.1:p.Pro1398ArgfsTer?
NM_001142768.1:c.4247del NP_001136240.1:p.Pro1416ArgfsTer?
NM_001142769.1:c.4349del NP_001136241.1:p.Pro1450ArgfsTer?
NM_001142770.1:c.4313del NP_001136242.1:p.Pro1438ArgfsTer29
NM_001142771.1:c.4328del NP_001136243.1:p.Pro1443ArgfsTer?
NM_001142772.1:c.4313del NP_001136244.1:p.Pro1438ArgfsTer?
NM_001142773.1:c.4238del NP_001136245.1:p.Pro1413ArgfsTer?
NM_033056.3:c.4313del NP_149045.3:p.Pro1438ArgfsTer?
NM_001142769.2:c.4349del NP_001136241.1:p.Pro1450ArgfsTer?
NM_001142770.2:c.4313del NP_001136242.1:p.Pro1438ArgfsTer29
NM_001354404.1:c.4247del NP_001341333.1:p.Pro1416ArgfsTer?
NM_001354411.1:c.4334del NP_001341340.1:p.Pro1445ArgfsTer?
NM_001354420.1:c.4313del NP_001341349.1:p.Pro1438ArgfsTer?
NM_001354429.1:c.4313del NP_001341358.1:p.Pro1438ArgfsTer19
XM_017016573.2:c.4328del XP_016872062.1:p.Pro1443ArgfsTer?
XR_001747192.2:n.5326del
XR_001747193.2:n.5317del
NM_001142763.2:c.4328del NP_001136235.1:p.Pro1443ArgfsTer?
NM_001142764.2:c.4313del NP_001136236.1:p.Pro1438ArgfsTer?
NM_001142765.2:c.4100del NP_001136237.1:p.Pro1367ArgfsTer?
NM_001142766.2:c.4304del NP_001136238.1:p.Pro1435ArgfsTer?
NM_001142768.2:c.4247del NP_001136240.1:p.Pro1416ArgfsTer?
NM_001142769.3:c.4349del NP_001136241.1:p.Pro1450ArgfsTer?
NM_001142770.3:c.4313del NP_001136242.1:p.Pro1438ArgfsTer29
NM_001142771.2:c.4328del NP_001136243.1:p.Pro1443ArgfsTer?
NM_001142772.2:c.4313del NP_001136244.1:p.Pro1438ArgfsTer?
NM_001142773.2:c.4238del NP_001136245.1:p.Pro1413ArgfsTer?
NM_001354411.2:c.4334del NP_001341340.1:p.Pro1445ArgfsTer?
NM_001354420.2:c.4313del NP_001341349.1:p.Pro1438ArgfsTer?
NM_001354429.2:c.4313del NP_001341358.1:p.Pro1438ArgfsTer19
NM_033056.4:c.4313del MANE Plus Clinical NP_149045.3:p.Pro1438ArgfsTer?
NM_001142767.2:c.4193del NP_001136239.1:p.Pro1398ArgfsTer?
NM_001354404.2:c.4247del NP_001341333.1:p.Pro1416ArgfsTer?
NM_001384140.1:c.4313del MANE Select NP_001371069.1:p.Pro1438ArgfsTer30