Canonical Allele Identifier: CA376525046

Gene: PCDH15

Linked Data

• MyVariant Identifiers: chr10:g.55582099A>G (hg19) ; chr10:g.53822339A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53822339A>G , CM000672.2:g.53822339A>G	GRCh38
NC_000010.10:g.55582099A>G , CM000672.1:g.55582099A>G	GRCh37
NC_000010.9:g.55252105A>G	NCBI36
NG_009191.2:g.983953T>C
NG_009191.3:g.1811844T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613657.6:c.4409+2797T>C	ENSP00000482794.1:n.4409+2797T>C
ENST00000320301.11:c.5387T>C MANE Plus Clinical	ENSP00000322604.6:p.Phe1796Ser
ENST00000395445.6:c.4388+5054T>C	ENSP00000378832.2:n.4388+5054T>C
ENST00000613657.5:c.4409+2797T>C	ENSP00000482794.1:n.4409+2797T>C
ENST00000642496.1:c.3227-2109T>C
ENST00000644397.2:c.4368-2109T>C MANE Select	ENSP00000495195.1:n.4368-2109T>C
ENST00000320301.10:c.5387T>C	ENSP00000322604.6:p.Phe1796Ser
ENST00000361849.7:c.5393T>C	ENSP00000354950.3:p.Phe1798Ser
ENST00000373956.7:c.*3342T>C	ENSP00000363067.4:n.*3342T>C
ENST00000373957.7:c.5408T>C	ENSP00000363068.4:p.Phe1803Ser
ENST00000373965.6:c.4373+2797T>C	ENSP00000363076.3:n.4373+2797T>C
ENST00000395430.5:c.5378T>C	ENSP00000378818.1:p.Phe1793Ser
ENST00000395432.6:c.5267T>C	ENSP00000378820.2:p.Phe1756Ser
ENST00000395433.5:c.5318T>C	ENSP00000378821.1:p.Phe1773Ser
ENST00000395438.5:c.4371+5053T>C	ENSP00000378826.2:n.4371+5053T>C
ENST00000395440.5:c.1306-12793T>C	ENSP00000378827.1:n.1306-12793T>C
ENST00000395442.5:c.1099-12793T>C	ENSP00000378829.1:n.1099-12793T>C
ENST00000395445.5:c.4388+5054T>C	ENSP00000378832.2:n.4388+5054T>C
ENST00000395446.5:c.2092-12793T>C	ENSP00000378833.1:n.2092-12793T>C
ENST00000409834.5:c.3206+2797T>C	ENSP00000386693.1:n.3206+2797T>C
ENST00000414367.5:c.*447+5054T>C	ENSP00000412531.1:n.*447+5054T>C
ENST00000414778.5:c.4370+5054T>C	ENSP00000410304.2:n.4370+5054T>C
ENST00000437009.5:c.5180T>C	ENSP00000412628.2:p.Phe1727Ser
ENST00000448885.5:c.*3348T>C	ENSP00000412320.1:n.*3348T>C
ENST00000463095.2:n.2406T>C
ENST00000495484.5:c.462-4326T>C	ENSP00000480780.1:n.462-4326T>C
ENST00000612394.4:c.4406+5054T>C	ENSP00000482921.1:n.4406+5054T>C
ENST00000613657.4:c.4409+2797T>C	ENSP00000482794.1:n.4409+2797T>C
ENST00000614895.4:c.4385+5054T>C	ENSP00000478512.1:n.4385+5054T>C
ENST00000616114.4:c.4367+5054T>C	ENSP00000483745.1:n.4367+5054T>C
ENST00000617051.4:c.5414T>C	ENSP00000484703.1:p.Phe1805Ser
ENST00000617271.4:c.4373+2797T>C	ENSP00000478076.1:n.4373+2797T>C
ENST00000618301.4:c.594-4326T>C	ENSP00000482780.1:n.594-4326T>C
ENST00000621708.4:c.4388+2797T>C	ENSP00000484454.1:n.4388+2797T>C
ENST00000622048.4:c.5186T>C	ENSP00000482329.1:p.Phe1729Ser
NM_001142763.1:c.5408T>C	NP_001136235.1:p.Phe1803Ser
NM_001142764.1:c.5393T>C	NP_001136236.1:p.Phe1798Ser
NM_001142765.1:c.5180T>C	NP_001136237.1:p.Phe1727Ser
NM_001142766.1:c.5378T>C	NP_001136238.1:p.Phe1793Ser
NM_001142767.1:c.5267T>C	NP_001136239.1:p.Phe1756Ser
NM_001142768.1:c.5327T>C	NP_001136240.1:p.Phe1776Ser
NM_001142769.1:c.4409+2797T>C	NP_001136241.1:n.4409+2797T>C
NM_001142770.1:c.4373+2797T>C	NP_001136242.1:n.4373+2797T>C
NM_001142771.1:c.4388+2797T>C	NP_001136243.1:n.4388+2797T>C
NM_001142772.1:c.4373+2797T>C	NP_001136244.1:n.4373+2797T>C
NM_001142773.1:c.5318T>C	NP_001136245.1:p.Phe1773Ser
NM_033056.3:c.5387T>C	NP_149045.3:p.Phe1796Ser
NM_001142769.2:c.4409+2797T>C	NP_001136241.1:n.4409+2797T>C
NM_001142770.2:c.4373+2797T>C	NP_001136242.1:n.4373+2797T>C
NM_001354404.1:c.5321T>C	NP_001341333.1:p.Phe1774Ser
NM_001354411.1:c.4388+5054T>C	NP_001341340.1:n.4388+5054T>C
NM_001354420.1:c.4367+5054T>C	NP_001341349.1:n.4367+5054T>C
NM_001354429.1:c.4368-4326T>C	NP_001341358.1:n.4368-4326T>C
XM_017016573.2:c.4388+2797T>C	XP_016872062.1:n.4388+2797T>C
XR_001747192.2:n.6400T>C
XR_001747193.2:n.6391T>C
NM_001142763.2:c.5408T>C	NP_001136235.1:p.Phe1803Ser
NM_001142764.2:c.5393T>C	NP_001136236.1:p.Phe1798Ser
NM_001142765.2:c.5180T>C	NP_001136237.1:p.Phe1727Ser
NM_001142766.2:c.5378T>C	NP_001136238.1:p.Phe1793Ser
NM_001142768.2:c.5327T>C	NP_001136240.1:p.Phe1776Ser
NM_001142769.3:c.4409+2797T>C	NP_001136241.1:n.4409+2797T>C
NM_001142770.3:c.4373+2797T>C	NP_001136242.1:n.4373+2797T>C
NM_001142771.2:c.4388+2797T>C	NP_001136243.1:n.4388+2797T>C
NM_001142772.2:c.4373+2797T>C	NP_001136244.1:n.4373+2797T>C
NM_001142773.2:c.5318T>C	NP_001136245.1:p.Phe1773Ser
NM_001354411.2:c.4388+5054T>C	NP_001341340.1:n.4388+5054T>C
NM_001354420.2:c.4367+5054T>C	NP_001341349.1:n.4367+5054T>C
NM_001354429.2:c.4368-4326T>C	NP_001341358.1:n.4368-4326T>C
NM_033056.4:c.5387T>C MANE Plus Clinical	NP_149045.3:p.Phe1796Ser
NM_001142767.2:c.5267T>C	NP_001136239.1:p.Phe1756Ser
NM_001354404.2:c.5321T>C	NP_001341333.1:p.Phe1774Ser
NM_001384140.1:c.4368-2109T>C MANE Select	NP_001371069.1:n.4368-2109T>C