Canonical Allele Identifier: CA376520553

Gene: PCDH15

Linked Data

• gnomAD v4: 10-53809358-G-C
• MyVariant Identifiers: chr10:g.55569118G>C (hg19) ; chr10:g.53809358G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53809358G>C , CM000672.2:g.53809358G>C	GRCh38
NC_000010.10:g.55569118G>C , CM000672.1:g.55569118G>C	GRCh37
NC_000010.9:g.55239124G>C	NCBI36
NG_009191.2:g.996934C>G
NG_009191.3:g.1824825C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613657.6:c.4707C>G	ENSP00000482794.1:p.Asp1569Glu
ENST00000395445.6:c.4686C>G	ENSP00000378832.2:p.Asp1562Glu
ENST00000613657.5:c.4707C>G	ENSP00000482794.1:p.Asp1569Glu
ENST00000642496.1:c.3530+1198C>G
ENST00000644397.2:c.4671+1198C>G MANE Select	ENSP00000495195.1:n.4671+1198C>G
ENST00000373965.6:c.4482+1198C>G	ENSP00000363076.3:n.4482+1198C>G
ENST00000395438.5:c.*122C>G	ENSP00000378826.2:n.*122C>G
ENST00000395440.5:c.1494C>G	ENSP00000378827.1:p.Asp498Glu
ENST00000395442.5:c.1287C>G	ENSP00000378829.1:p.Asp429Glu
ENST00000395445.5:c.4686C>G	ENSP00000378832.2:p.Asp1562Glu
ENST00000395446.5:c.2280C>G	ENSP00000378833.1:p.Asp760Glu
ENST00000409834.5:c.*122C>G	ENSP00000386693.1:n.*122C>G
ENST00000414367.5:c.*745C>G	ENSP00000412531.1:n.*745C>G
ENST00000414778.5:c.4479+1198C>G	ENSP00000410304.2:n.4479+1198C>G
ENST00000476074.5:n.609+1198C>G
ENST00000495484.5:c.699+1198C>G	ENSP00000480780.1:n.699+1198C>G
ENST00000612394.4:c.4704C>G	ENSP00000482921.1:p.Asp1568Glu
ENST00000613657.4:c.4707C>G	ENSP00000482794.1:p.Asp1569Glu
ENST00000614895.4:c.4494+1198C>G	ENSP00000478512.1:n.4494+1198C>G
ENST00000615043.1:c.307C>G
ENST00000616114.4:c.4476+1198C>G	ENSP00000483745.1:n.4476+1198C>G
ENST00000617271.4:c.*122C>G	ENSP00000478076.1:n.*122C>G
ENST00000618301.4:c.831+1198C>G	ENSP00000482780.1:n.831+1198C>G
ENST00000621708.4:c.4497+1198C>G	ENSP00000484454.1:n.4497+1198C>G
NM_001142769.1:c.4707C>G	NP_001136241.1:p.Asp1569Glu
NM_001142770.1:c.*122C>G	NP_001136242.1:n.*122C>G
NM_001142771.1:c.4497+1198C>G	NP_001136243.1:n.4497+1198C>G
NM_001142772.1:c.4482+1198C>G	NP_001136244.1:n.4482+1198C>G
NM_001142769.2:c.4707C>G	NP_001136241.1:p.Asp1569Glu
NM_001142770.2:c.*122C>G	NP_001136242.1:n.*122C>G
NM_001354411.1:c.4686C>G	NP_001341340.1:p.Asp1562Glu
NM_001354420.1:c.4476+1198C>G	NP_001341349.1:n.4476+1198C>G
NM_001354429.1:c.4605+1198C>G	NP_001341358.1:n.4605+1198C>G
XM_017016573.2:c.4686C>G	XP_016872062.1:p.Asp1562Glu
XR_001747192.2:n.10963+1198C>G
XR_001747193.2:n.10954+1198C>G
NM_001142769.3:c.4707C>G	NP_001136241.1:p.Asp1569Glu
NM_001142770.3:c.*122C>G	NP_001136242.1:n.*122C>G
NM_001142771.2:c.4497+1198C>G	NP_001136243.1:n.4497+1198C>G
NM_001142772.2:c.4482+1198C>G	NP_001136244.1:n.4482+1198C>G
NM_001354411.2:c.4686C>G	NP_001341340.1:p.Asp1562Glu
NM_001354420.2:c.4476+1198C>G	NP_001341349.1:n.4476+1198C>G
NM_001354429.2:c.4605+1198C>G	NP_001341358.1:n.4605+1198C>G
NM_001384140.1:c.4671+1198C>G MANE Select	NP_001371069.1:n.4671+1198C>G