Canonical Allele Identifier: CA376515772

Gene: PCDH15

Linked Data

• MyVariant Identifiers: chr10:g.55566386A>C (hg19) ; chr10:g.53806626A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806626A>C , CM000672.2:g.53806626A>C	GRCh38
NC_000010.10:g.55566386A>C , CM000672.1:g.55566386A>C	GRCh37
NC_000010.9:g.55236392A>C	NCBI36
NG_009191.2:g.999666T>G
NG_009191.3:g.1827557T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642496.1:c.4035T>G
ENST00000644397.2:c.5176T>G MANE Select	ENSP00000495195.1:p.Trp1726Gly
ENST00000373965.6:c.4987T>G	ENSP00000363076.3:p.Trp1663Gly
ENST00000414778.5:c.4984T>G	ENSP00000410304.2:p.Trp1662Gly
ENST00000495484.5:c.1204T>G	ENSP00000480780.1:p.Trp402Gly
ENST00000614895.4:c.4999T>G	ENSP00000478512.1:p.Trp1667Gly
ENST00000616114.4:c.4981T>G	ENSP00000483745.1:p.Trp1661Gly
ENST00000618301.4:c.1336T>G	ENSP00000482780.1:p.Trp446Gly
ENST00000621708.4:c.5002T>G	ENSP00000484454.1:p.Trp1668Gly
NM_001142771.1:c.5002T>G	NP_001136243.1:p.Trp1668Gly
NM_001142772.1:c.4987T>G	NP_001136244.1:p.Trp1663Gly
NM_001354420.1:c.4981T>G	NP_001341349.1:p.Trp1661Gly
NM_001354429.1:c.5110T>G	NP_001341358.1:p.Trp1704Gly
XR_001747192.2:n.11468T>G
XR_001747193.2:n.11459T>G
NM_001142771.2:c.5002T>G	NP_001136243.1:p.Trp1668Gly
NM_001142772.2:c.4987T>G	NP_001136244.1:p.Trp1663Gly
NM_001354420.2:c.4981T>G	NP_001341349.1:p.Trp1661Gly
NM_001354429.2:c.5110T>G	NP_001341358.1:p.Trp1704Gly
NM_001384140.1:c.5176T>G MANE Select	NP_001371069.1:p.Trp1726Gly