Canonical Allele Identifier: CA376519616

Gene: PCDH15

Linked Data

• MyVariant Identifiers: chr10:g.55568798A>G (hg19) ; chr10:g.53809038A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53809038A>G , CM000672.2:g.53809038A>G	GRCh38
NC_000010.10:g.55568798A>G , CM000672.1:g.55568798A>G	GRCh37
NC_000010.9:g.55238804A>G	NCBI36
NG_009191.2:g.997254T>C
NG_009191.3:g.1825145T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613657.6:c.5027T>C	ENSP00000482794.1:p.Val1676Ala
ENST00000395445.6:c.5006T>C	ENSP00000378832.2:p.Val1669Ala
ENST00000613657.5:c.5027T>C	ENSP00000482794.1:p.Val1676Ala
ENST00000642496.1:c.3530+1518T>C
ENST00000644397.2:c.4671+1518T>C MANE Select	ENSP00000495195.1:n.4671+1518T>C
ENST00000373965.6:c.4482+1518T>C	ENSP00000363076.3:n.4482+1518T>C
ENST00000395438.5:c.*442T>C	ENSP00000378826.2:n.*442T>C
ENST00000395440.5:c.1814T>C	ENSP00000378827.1:p.Val605Ala
ENST00000395442.5:c.1607T>C	ENSP00000378829.1:p.Val536Ala
ENST00000395445.5:c.5006T>C	ENSP00000378832.2:p.Val1669Ala
ENST00000395446.5:c.2600T>C	ENSP00000378833.1:p.Val867Ala
ENST00000409834.5:c.*442T>C	ENSP00000386693.1:n.*442T>C
ENST00000414367.5:c.*1065T>C	ENSP00000412531.1:n.*1065T>C
ENST00000414778.5:c.4479+1518T>C	ENSP00000410304.2:n.4479+1518T>C
ENST00000476074.5:n.609+1518T>C
ENST00000495484.5:c.699+1518T>C	ENSP00000480780.1:n.699+1518T>C
ENST00000612394.4:c.5024T>C	ENSP00000482921.1:p.Val1675Ala
ENST00000613657.4:c.5027T>C	ENSP00000482794.1:p.Val1676Ala
ENST00000614895.4:c.4494+1518T>C	ENSP00000478512.1:n.4494+1518T>C
ENST00000615043.1:c.627T>C
ENST00000616114.4:c.4476+1518T>C	ENSP00000483745.1:n.4476+1518T>C
ENST00000617271.4:c.*442T>C	ENSP00000478076.1:n.*442T>C
ENST00000618301.4:c.831+1518T>C	ENSP00000482780.1:n.831+1518T>C
ENST00000621708.4:c.4497+1518T>C	ENSP00000484454.1:n.4497+1518T>C
NM_001142769.1:c.5027T>C	NP_001136241.1:p.Val1676Ala
NM_001142770.1:c.*442T>C	NP_001136242.1:n.*442T>C
NM_001142771.1:c.4497+1518T>C	NP_001136243.1:n.4497+1518T>C
NM_001142772.1:c.4482+1518T>C	NP_001136244.1:n.4482+1518T>C
NM_001142769.2:c.5027T>C	NP_001136241.1:p.Val1676Ala
NM_001142770.2:c.*442T>C	NP_001136242.1:n.*442T>C
NM_001354411.1:c.5006T>C	NP_001341340.1:p.Val1669Ala
NM_001354420.1:c.4476+1518T>C	NP_001341349.1:n.4476+1518T>C
NM_001354429.1:c.4605+1518T>C	NP_001341358.1:n.4605+1518T>C
XM_017016573.2:c.5006T>C	XP_016872062.1:p.Val1669Ala
XR_001747192.2:n.10963+1518T>C
XR_001747193.2:n.10954+1518T>C
NM_001142769.3:c.5027T>C	NP_001136241.1:p.Val1676Ala
NM_001142770.3:c.*442T>C	NP_001136242.1:n.*442T>C
NM_001142771.2:c.4497+1518T>C	NP_001136243.1:n.4497+1518T>C
NM_001142772.2:c.4482+1518T>C	NP_001136244.1:n.4482+1518T>C
NM_001354411.2:c.5006T>C	NP_001341340.1:p.Val1669Ala
NM_001354420.2:c.4476+1518T>C	NP_001341349.1:n.4476+1518T>C
NM_001354429.2:c.4605+1518T>C	NP_001341358.1:n.4605+1518T>C
NM_001384140.1:c.4671+1518T>C MANE Select	NP_001371069.1:n.4671+1518T>C