Canonical Allele Identifier: CA2788045223

Gene: PCDH15

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.54195885_54195901del , CM000672.2:g.54195885_54195901del	GRCh38
NC_000010.10:g.55955645_55955661del , CM000672.1:g.55955645_55955661del	GRCh37
NC_000010.9:g.55625651_55625667del	NCBI36
NG_009191.2:g.610391_610407del
NG_009191.3:g.1438282_1438298del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613657.6:c.1114-12_1118del
ENST00000320301.11:c.1099-12_1103del
ENST00000395445.6:c.1099-12_1103del
ENST00000613657.5:c.1114-12_1118del
ENST00000644397.2:c.1099-12_1103del
ENST00000320301.10:c.1099-12_1103del
ENST00000361849.7:c.1099-12_1103del
ENST00000373955.5:c.1099-12_1103del
ENST00000373956.7:c.1099-12_1103del
ENST00000373957.7:c.1114-12_1118del
ENST00000373965.6:c.1099-12_1103del
ENST00000395430.5:c.1099-12_1103del
ENST00000395432.6:c.988-12_992del
ENST00000395433.5:c.1033-12_1037del
ENST00000395438.5:c.1099-12_1103del
ENST00000395440.5:c.1099-12_1103del
ENST00000395442.5:c.1098+18035_1098+18051del	ENSP00000378829.1:n.1098+18035_1098+18051del
ENST00000395445.5:c.1099-12_1103del
ENST00000395446.5:c.1099-12_1103del
ENST00000409834.5:c.-90-12_-86del
ENST00000414367.5:c.876+121370_876+121386del	ENSP00000412531.1:n.876+121370_876+121386del
ENST00000414778.5:c.1099-12_1103del
ENST00000437009.5:c.1099-12_1103del
ENST00000448885.5:c.1099-12_1103del
ENST00000495484.5:c.-24-338638_-24-338622del	ENSP00000480780.1:n.-24-338638_-24-338622del
ENST00000612394.4:c.1114-12_1118del
ENST00000613657.4:c.1114-12_1118del
ENST00000614895.4:c.1114-12_1118del
ENST00000616114.4:c.1099-12_1103del
ENST00000617051.4:c.1114-12_1118del
ENST00000617271.4:c.1099-12_1103del
ENST00000621708.4:c.1114-12_1118del
ENST00000622048.4:c.1099-12_1103del
NM_001142763.1:c.1114-12_1118del
NM_001142764.1:c.1099-12_1103del
NM_001142765.1:c.1099-12_1103del
NM_001142766.1:c.1099-12_1103del
NM_001142767.1:c.988-12_992del
NM_001142768.1:c.1033-12_1037del
NM_001142769.1:c.1114-12_1118del
NM_001142770.1:c.1099-12_1103del
NM_001142771.1:c.1114-12_1118del
NM_001142772.1:c.1099-12_1103del
NM_001142773.1:c.1033-12_1037del
NM_033056.3:c.1099-12_1103del
NM_001142769.2:c.1114-12_1118del
NM_001142770.2:c.1099-12_1103del
NM_001354404.1:c.1033-12_1037del
NM_001354411.1:c.1099-12_1103del
NM_001354420.1:c.1099-12_1103del
NM_001354429.1:c.1099-12_1103del
NM_001354430.1:c.1099-12_1103del
XM_017016573.2:c.1114-12_1118del
XR_001747192.2:n.2112-12_2116del
XR_001747193.2:n.2112-12_2116del
NM_001142763.2:c.1114-12_1118del
NM_001142764.2:c.1099-12_1103del
NM_001142765.2:c.1099-12_1103del
NM_001142766.2:c.1099-12_1103del
NM_001142768.2:c.1033-12_1037del
NM_001142769.3:c.1114-12_1118del
NM_001142770.3:c.1099-12_1103del
NM_001142771.2:c.1114-12_1118del
NM_001142772.2:c.1099-12_1103del
NM_001142773.2:c.1033-12_1037del
NM_001354411.2:c.1099-12_1103del
NM_001354420.2:c.1099-12_1103del
NM_001354429.2:c.1099-12_1103del
NM_001354430.2:c.1099-12_1103del
NM_033056.4:c.1099-12_1103del
NM_001142767.2:c.988-12_992del
NM_001354404.2:c.1033-12_1037del
NM_001384140.1:c.1099-12_1103del