Canonical Allele Identifier: CA2788034652
Gene: PCDH15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.53809440_53809441insTGG , CM000672.2:g.53809440_53809441insTGG GRCh38
NC_000010.10:g.55569200_55569201insTGG , CM000672.1:g.55569200_55569201insTGG GRCh37
NC_000010.9:g.55239206_55239207insTGG NCBI36
NG_009191.2:g.996851_996852insCCA
NG_009191.3:g.1824742_1824743insCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000613657.6:c.4624_4625insCCA ENSP00000482794.1:p.Tyr1542delinsSerAsn
ENST00000395445.6:c.4603_4604insCCA ENSP00000378832.2:p.Tyr1535delinsSerAsn
ENST00000613657.5:c.4624_4625insCCA ENSP00000482794.1:p.Tyr1542delinsSerAsn
ENST00000642496.1:c.3530+1115_3530+1116insCCA
ENST00000644397.2:c.4671+1115_4671+1116insCCA MANE Select ENSP00000495195.1:n.4671+1115_4671+1116insCCA
ENST00000373965.6:c.4482+1115_4482+1116insCCA ENSP00000363076.3:n.4482+1115_4482+1116insCCA
ENST00000395438.5:c.*39_*40insCCA ENSP00000378826.2:n.*39_*40insCCA
ENST00000395440.5:c.1411_1412insCCA ENSP00000378827.1:p.Tyr471delinsSerAsn
ENST00000395442.5:c.1204_1205insCCA ENSP00000378829.1:p.Tyr402delinsSerAsn
ENST00000395445.5:c.4603_4604insCCA ENSP00000378832.2:p.Tyr1535delinsSerAsn
ENST00000395446.5:c.2197_2198insCCA ENSP00000378833.1:p.Tyr733delinsSerAsn
ENST00000409834.5:c.*39_*40insCCA ENSP00000386693.1:n.*39_*40insCCA
ENST00000414367.5:c.*662_*663insCCA ENSP00000412531.1:n.*662_*663insCCA
ENST00000414778.5:c.4479+1115_4479+1116insCCA ENSP00000410304.2:n.4479+1115_4479+1116insCCA
ENST00000476074.5:n.609+1115_609+1116insCCA
ENST00000495484.5:c.699+1115_699+1116insCCA ENSP00000480780.1:n.699+1115_699+1116insCCA
ENST00000612394.4:c.4621_4622insCCA ENSP00000482921.1:p.Tyr1541delinsSerAsn
ENST00000613657.4:c.4624_4625insCCA ENSP00000482794.1:p.Tyr1542delinsSerAsn
ENST00000614895.4:c.4494+1115_4494+1116insCCA ENSP00000478512.1:n.4494+1115_4494+1116insCCA
ENST00000615043.1:c.224_225insCCA
ENST00000616114.4:c.4476+1115_4476+1116insCCA ENSP00000483745.1:n.4476+1115_4476+1116insCCA
ENST00000617271.4:c.*39_*40insCCA ENSP00000478076.1:n.*39_*40insCCA
ENST00000618301.4:c.831+1115_831+1116insCCA ENSP00000482780.1:n.831+1115_831+1116insCCA
ENST00000621708.4:c.4497+1115_4497+1116insCCA ENSP00000484454.1:n.4497+1115_4497+1116insCCA
NM_001142769.1:c.4624_4625insCCA NP_001136241.1:p.Tyr1542delinsSerAsn
NM_001142770.1:c.*39_*40insCCA NP_001136242.1:n.*39_*40insCCA
NM_001142771.1:c.4497+1115_4497+1116insCCA NP_001136243.1:n.4497+1115_4497+1116insCCA
NM_001142772.1:c.4482+1115_4482+1116insCCA NP_001136244.1:n.4482+1115_4482+1116insCCA
NM_001142769.2:c.4624_4625insCCA NP_001136241.1:p.Tyr1542delinsSerAsn
NM_001142770.2:c.*39_*40insCCA NP_001136242.1:n.*39_*40insCCA
NM_001354411.1:c.4603_4604insCCA NP_001341340.1:p.Tyr1535delinsSerAsn
NM_001354420.1:c.4476+1115_4476+1116insCCA NP_001341349.1:n.4476+1115_4476+1116insCCA
NM_001354429.1:c.4605+1115_4605+1116insCCA NP_001341358.1:n.4605+1115_4605+1116insCCA
XM_017016573.2:c.4603_4604insCCA XP_016872062.1:p.Tyr1535delinsSerAsn
XR_001747192.2:n.10963+1115_10963+1116insCCA
XR_001747193.2:n.10954+1115_10954+1116insCCA
NM_001142769.3:c.4624_4625insCCA NP_001136241.1:p.Tyr1542delinsSerAsn
NM_001142770.3:c.*39_*40insCCA NP_001136242.1:n.*39_*40insCCA
NM_001142771.2:c.4497+1115_4497+1116insCCA NP_001136243.1:n.4497+1115_4497+1116insCCA
NM_001142772.2:c.4482+1115_4482+1116insCCA NP_001136244.1:n.4482+1115_4482+1116insCCA
NM_001354411.2:c.4603_4604insCCA NP_001341340.1:p.Tyr1535delinsSerAsn
NM_001354420.2:c.4476+1115_4476+1116insCCA NP_001341349.1:n.4476+1115_4476+1116insCCA
NM_001354429.2:c.4605+1115_4605+1116insCCA NP_001341358.1:n.4605+1115_4605+1116insCCA
NM_001384140.1:c.4671+1115_4671+1116insCCA MANE Select NP_001371069.1:n.4671+1115_4671+1116insCCA