Canonical Allele Identifier: CA376520693

Gene: PCDH15

Linked Data

• dbSNP Id: rs1422408762
• MyVariant Identifiers: chr10:g.55719492C>G (hg19) ; chr10:g.53959732C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53959732C>G , CM000672.2:g.53959732C>G	GRCh38
NC_000010.10:g.55719492C>G , CM000672.1:g.55719492C>G	GRCh37
NC_000010.9:g.55389498C>G	NCBI36
NG_009191.2:g.846560G>C
NG_009191.3:g.1674451G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000613657.6:c.3158G>C	ENSP00000482794.1:p.Arg1053Thr
ENST00000320301.11:c.3122G>C MANE Plus Clinical	ENSP00000322604.6:p.Arg1041Thr
ENST00000395445.6:c.3143G>C	ENSP00000378832.2:p.Arg1048Thr
ENST00000613657.5:c.3158G>C	ENSP00000482794.1:p.Arg1053Thr
ENST00000642496.1:c.1981G>C
ENST00000644397.2:c.3122G>C MANE Select	ENSP00000495195.1:p.Arg1041Thr
ENST00000320301.10:c.3122G>C	ENSP00000322604.6:p.Arg1041Thr
ENST00000361849.7:c.3122G>C	ENSP00000354950.3:p.Arg1041Thr
ENST00000373956.7:c.*1077G>C	ENSP00000363067.4:n.*1077G>C
ENST00000373957.7:c.3137G>C	ENSP00000363068.4:p.Arg1046Thr
ENST00000373965.6:c.3122G>C	ENSP00000363076.3:p.Arg1041Thr
ENST00000395430.5:c.3122G>C	ENSP00000378818.1:p.Arg1041Thr
ENST00000395432.6:c.3011G>C	ENSP00000378820.2:p.Arg1004Thr
ENST00000395433.5:c.3056G>C	ENSP00000378821.1:p.Arg1019Thr
ENST00000395438.5:c.3122G>C	ENSP00000378826.2:p.Arg1041Thr
ENST00000395440.5:c.1306-150186G>C	ENSP00000378827.1:n.1306-150186G>C
ENST00000395442.5:c.1099-150186G>C	ENSP00000378829.1:n.1099-150186G>C
ENST00000395445.5:c.3143G>C	ENSP00000378832.2:p.Arg1048Thr
ENST00000395446.5:c.2091+119599G>C	ENSP00000378833.1:n.2091+119599G>C
ENST00000409834.5:c.1955G>C	ENSP00000386693.1:p.Arg652Thr
ENST00000414367.5:c.877-119236G>C	ENSP00000412531.1:n.877-119236G>C
ENST00000414778.5:c.3122G>C	ENSP00000410304.2:p.Arg1041Thr
ENST00000437009.5:c.2909G>C	ENSP00000412628.2:p.Arg970Thr
ENST00000448885.5:c.*1077G>C	ENSP00000412320.1:n.*1077G>C
ENST00000495484.5:c.-24-102469G>C	ENSP00000480780.1:n.-24-102469G>C
ENST00000612394.4:c.3158G>C	ENSP00000482921.1:p.Arg1053Thr
ENST00000613657.4:c.3158G>C	ENSP00000482794.1:p.Arg1053Thr
ENST00000614895.4:c.3137G>C	ENSP00000478512.1:p.Arg1046Thr
ENST00000616114.4:c.3122G>C	ENSP00000483745.1:p.Arg1041Thr
ENST00000617051.4:c.3137G>C	ENSP00000484703.1:p.Arg1046Thr
ENST00000617271.4:c.3122G>C	ENSP00000478076.1:p.Arg1041Thr
ENST00000621708.4:c.3137G>C	ENSP00000484454.1:p.Arg1046Thr
ENST00000622048.4:c.2909G>C	ENSP00000482329.1:p.Arg970Thr
NM_001142763.1:c.3137G>C	NP_001136235.1:p.Arg1046Thr
NM_001142764.1:c.3122G>C	NP_001136236.1:p.Arg1041Thr
NM_001142765.1:c.2909G>C	NP_001136237.1:p.Arg970Thr
NM_001142766.1:c.3122G>C	NP_001136238.1:p.Arg1041Thr
NM_001142767.1:c.3011G>C	NP_001136239.1:p.Arg1004Thr
NM_001142768.1:c.3056G>C	NP_001136240.1:p.Arg1019Thr
NM_001142769.1:c.3158G>C	NP_001136241.1:p.Arg1053Thr
NM_001142770.1:c.3122G>C	NP_001136242.1:p.Arg1041Thr
NM_001142771.1:c.3137G>C	NP_001136243.1:p.Arg1046Thr
NM_001142772.1:c.3122G>C	NP_001136244.1:p.Arg1041Thr
NM_001142773.1:c.3056G>C	NP_001136245.1:p.Arg1019Thr
NM_033056.3:c.3122G>C	NP_149045.3:p.Arg1041Thr
NM_001142769.2:c.3158G>C	NP_001136241.1:p.Arg1053Thr
NM_001142770.2:c.3122G>C	NP_001136242.1:p.Arg1041Thr
NM_001354404.1:c.3056G>C	NP_001341333.1:p.Arg1019Thr
NM_001354411.1:c.3143G>C	NP_001341340.1:p.Arg1048Thr
NM_001354420.1:c.3122G>C	NP_001341349.1:p.Arg1041Thr
NM_001354429.1:c.3122G>C	NP_001341358.1:p.Arg1041Thr
XM_017016573.2:c.3137G>C	XP_016872062.1:p.Arg1046Thr
XR_001747192.2:n.4135G>C
XR_001747193.2:n.4135G>C
NM_001142763.2:c.3137G>C	NP_001136235.1:p.Arg1046Thr
NM_001142764.2:c.3122G>C	NP_001136236.1:p.Arg1041Thr
NM_001142765.2:c.2909G>C	NP_001136237.1:p.Arg970Thr
NM_001142766.2:c.3122G>C	NP_001136238.1:p.Arg1041Thr
NM_001142768.2:c.3056G>C	NP_001136240.1:p.Arg1019Thr
NM_001142769.3:c.3158G>C	NP_001136241.1:p.Arg1053Thr
NM_001142770.3:c.3122G>C	NP_001136242.1:p.Arg1041Thr
NM_001142771.2:c.3137G>C	NP_001136243.1:p.Arg1046Thr
NM_001142772.2:c.3122G>C	NP_001136244.1:p.Arg1041Thr
NM_001142773.2:c.3056G>C	NP_001136245.1:p.Arg1019Thr
NM_001354411.2:c.3143G>C	NP_001341340.1:p.Arg1048Thr
NM_001354420.2:c.3122G>C	NP_001341349.1:p.Arg1041Thr
NM_001354429.2:c.3122G>C	NP_001341358.1:p.Arg1041Thr
NM_033056.4:c.3122G>C MANE Plus Clinical	NP_149045.3:p.Arg1041Thr
NM_001142767.2:c.3011G>C	NP_001136239.1:p.Arg1004Thr
NM_001354404.2:c.3056G>C	NP_001341333.1:p.Arg1019Thr
NM_001384140.1:c.3122G>C MANE Select	NP_001371069.1:p.Arg1041Thr