Canonical Allele Identifier: CA2788035441

Gene: PCDH15

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53823807_53823830dup , CM000672.2:g.53823807_53823830dup	GRCh38
NC_000010.10:g.55583567_55583590dup , CM000672.1:g.55583567_55583590dup	GRCh37
NC_000010.9:g.55253573_55253596dup	NCBI36
NG_009191.2:g.982464_982487dup
NG_009191.3:g.1810355_1810378dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613657.6:c.4409+1308_4409+1331dup	ENSP00000482794.1:n.4409+1308_4409+1331dup
ENST00000320301.11:c.4368-470_4368-447dup MANE Plus Clinical	ENSP00000322604.6:n.4368-470_4368-447dup
ENST00000395445.6:c.4388+3565_4388+3588dup	ENSP00000378832.2:n.4388+3565_4388+3588dup
ENST00000613657.5:c.4409+1308_4409+1331dup	ENSP00000482794.1:n.4409+1308_4409+1331dup
ENST00000642496.1:c.3226+3565_3227-3575dup
ENST00000644397.2:c.4367+3565_4368-3575dup MANE Select	ENSP00000495195.1:n.4367+3565_4368-3575dup
ENST00000320301.10:c.4368-470_4368-447dup	ENSP00000322604.6:n.4368-470_4368-447dup
ENST00000361849.7:c.4374-470_4374-447dup	ENSP00000354950.3:n.4374-470_4374-447dup
ENST00000373956.7:c.*2323-470_*2323-447dup	ENSP00000363067.4:n.*2323-470_*2323-447dup
ENST00000373957.7:c.4389-470_4389-447dup	ENSP00000363068.4:n.4389-470_4389-447dup
ENST00000373965.6:c.4373+1308_4373+1331dup	ENSP00000363076.3:n.4373+1308_4373+1331dup
ENST00000395430.5:c.4359-470_4359-447dup	ENSP00000378818.1:n.4359-470_4359-447dup
ENST00000395432.6:c.4248-470_4248-447dup	ENSP00000378820.2:n.4248-470_4248-447dup
ENST00000395433.5:c.4299-470_4299-447dup	ENSP00000378821.1:n.4299-470_4299-447dup
ENST00000395438.5:c.4371+3564_4371+3587dup	ENSP00000378826.2:n.4371+3564_4371+3587dup
ENST00000395440.5:c.1306-14282_1306-14259dup	ENSP00000378827.1:n.1306-14282_1306-14259dup
ENST00000395442.5:c.1099-14282_1099-14259dup	ENSP00000378829.1:n.1099-14282_1099-14259dup
ENST00000395445.5:c.4388+3565_4388+3588dup	ENSP00000378832.2:n.4388+3565_4388+3588dup
ENST00000395446.5:c.2092-14282_2092-14259dup	ENSP00000378833.1:n.2092-14282_2092-14259dup
ENST00000409834.5:c.3206+1308_3206+1331dup	ENSP00000386693.1:n.3206+1308_3206+1331dup
ENST00000414367.5:c.*447+3565_*447+3588dup	ENSP00000412531.1:n.*447+3565_*447+3588dup
ENST00000414778.5:c.4370+3565_4370+3588dup	ENSP00000410304.2:n.4370+3565_4370+3588dup
ENST00000437009.5:c.4161-470_4161-447dup	ENSP00000412628.2:n.4161-470_4161-447dup
ENST00000448885.5:c.*2329-470_*2329-447dup	ENSP00000412320.1:n.*2329-470_*2329-447dup
ENST00000463095.2:n.1387-470_1387-447dup
ENST00000495484.5:c.462-5815_462-5792dup	ENSP00000480780.1:n.462-5815_462-5792dup
ENST00000612394.4:c.4406+3565_4406+3588dup	ENSP00000482921.1:n.4406+3565_4406+3588dup
ENST00000613657.4:c.4409+1308_4409+1331dup	ENSP00000482794.1:n.4409+1308_4409+1331dup
ENST00000614895.4:c.4385+3565_4385+3588dup	ENSP00000478512.1:n.4385+3565_4385+3588dup
ENST00000616114.4:c.4367+3565_4367+3588dup	ENSP00000483745.1:n.4367+3565_4367+3588dup
ENST00000617051.4:c.4386-461_4386-438dup	ENSP00000484703.1:n.4386-461_4386-438dup
ENST00000617271.4:c.4373+1308_4373+1331dup	ENSP00000478076.1:n.4373+1308_4373+1331dup
ENST00000618301.4:c.593+3565_593+3588dup	ENSP00000482780.1:n.593+3565_593+3588dup
ENST00000621708.4:c.4388+1308_4388+1331dup	ENSP00000484454.1:n.4388+1308_4388+1331dup
ENST00000622048.4:c.4158-461_4158-438dup	ENSP00000482329.1:n.4158-461_4158-438dup
NM_001142763.1:c.4389-470_4389-447dup	NP_001136235.1:n.4389-470_4389-447dup
NM_001142764.1:c.4374-470_4374-447dup	NP_001136236.1:n.4374-470_4374-447dup
NM_001142765.1:c.4161-470_4161-447dup	NP_001136237.1:n.4161-470_4161-447dup
NM_001142766.1:c.4359-470_4359-447dup	NP_001136238.1:n.4359-470_4359-447dup
NM_001142767.1:c.4248-470_4248-447dup	NP_001136239.1:n.4248-470_4248-447dup
NM_001142768.1:c.4308-470_4308-447dup	NP_001136240.1:n.4308-470_4308-447dup
NM_001142769.1:c.4409+1308_4409+1331dup	NP_001136241.1:n.4409+1308_4409+1331dup
NM_001142770.1:c.4373+1308_4373+1331dup	NP_001136242.1:n.4373+1308_4373+1331dup
NM_001142771.1:c.4388+1308_4388+1331dup	NP_001136243.1:n.4388+1308_4388+1331dup
NM_001142772.1:c.4373+1308_4373+1331dup	NP_001136244.1:n.4373+1308_4373+1331dup
NM_001142773.1:c.4299-470_4299-447dup	NP_001136245.1:n.4299-470_4299-447dup
NM_033056.3:c.4368-470_4368-447dup	NP_149045.3:n.4368-470_4368-447dup
NM_001142769.2:c.4409+1308_4409+1331dup	NP_001136241.1:n.4409+1308_4409+1331dup
NM_001142770.2:c.4373+1308_4373+1331dup	NP_001136242.1:n.4373+1308_4373+1331dup
NM_001354404.1:c.4302-470_4302-447dup	NP_001341333.1:n.4302-470_4302-447dup
NM_001354411.1:c.4388+3565_4388+3588dup	NP_001341340.1:n.4388+3565_4388+3588dup
NM_001354420.1:c.4367+3565_4367+3588dup	NP_001341349.1:n.4367+3565_4367+3588dup
NM_001354429.1:c.4367+3565_4367+3588dup	NP_001341358.1:n.4367+3565_4367+3588dup
XM_017016573.2:c.4388+1308_4388+1331dup	XP_016872062.1:n.4388+1308_4388+1331dup
XR_001747192.2:n.5381-470_5381-447dup
XR_001747193.2:n.5372-470_5372-447dup
NM_001142763.2:c.4389-470_4389-447dup	NP_001136235.1:n.4389-470_4389-447dup
NM_001142764.2:c.4374-470_4374-447dup	NP_001136236.1:n.4374-470_4374-447dup
NM_001142765.2:c.4161-470_4161-447dup	NP_001136237.1:n.4161-470_4161-447dup
NM_001142766.2:c.4359-470_4359-447dup	NP_001136238.1:n.4359-470_4359-447dup
NM_001142768.2:c.4308-470_4308-447dup	NP_001136240.1:n.4308-470_4308-447dup
NM_001142769.3:c.4409+1308_4409+1331dup	NP_001136241.1:n.4409+1308_4409+1331dup
NM_001142770.3:c.4373+1308_4373+1331dup	NP_001136242.1:n.4373+1308_4373+1331dup
NM_001142771.2:c.4388+1308_4388+1331dup	NP_001136243.1:n.4388+1308_4388+1331dup
NM_001142772.2:c.4373+1308_4373+1331dup	NP_001136244.1:n.4373+1308_4373+1331dup
NM_001142773.2:c.4299-470_4299-447dup	NP_001136245.1:n.4299-470_4299-447dup
NM_001354411.2:c.4388+3565_4388+3588dup	NP_001341340.1:n.4388+3565_4388+3588dup
NM_001354420.2:c.4367+3565_4367+3588dup	NP_001341349.1:n.4367+3565_4367+3588dup
NM_001354429.2:c.4367+3565_4367+3588dup	NP_001341358.1:n.4367+3565_4367+3588dup
NM_033056.4:c.4368-470_4368-447dup MANE Plus Clinical	NP_149045.3:n.4368-470_4368-447dup
NM_001142767.2:c.4248-470_4248-447dup	NP_001136239.1:n.4248-470_4248-447dup
NM_001354404.2:c.4302-470_4302-447dup	NP_001341333.1:n.4302-470_4302-447dup
NM_001384140.1:c.4367+3565_4368-3575dup MANE Select	NP_001371069.1:n.4367+3565_4368-3575dup