Canonical Allele Identifier: CA653310632

Gene: PCDH15

Linked Data

• dbSNP Id: rs1458642404
• gnomAD v4: 10-53806483-T-C
• COSMIC: COSN26440257
• MyVariant Identifiers: chr10:g.55566243T>C (hg19) ; chr10:g.53806483T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806483T>C , CM000672.2:g.53806483T>C	GRCh38
NC_000010.10:g.55566243T>C , CM000672.1:g.55566243T>C	GRCh37
NC_000010.9:g.55236249T>C	NCBI36
NG_009191.2:g.999809A>G
NG_009191.3:g.1827700A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642496.1:c.4178A>G
ENST00000644397.2:c.*96A>G MANE Select	ENSP00000495195.1:n.*96A>G
ENST00000373965.6:c.*96A>G	ENSP00000363076.3:n.*96A>G
ENST00000414778.5:c.*96A>G	ENSP00000410304.2:n.*96A>G
ENST00000495484.5:c.*96A>G	ENSP00000480780.1:n.*96A>G
ENST00000614895.4:c.*96A>G	ENSP00000478512.1:n.*96A>G
ENST00000616114.4:c.*96A>G	ENSP00000483745.1:n.*96A>G
ENST00000621708.4:c.*96A>G	ENSP00000484454.1:n.*96A>G
NM_001142771.1:c.*96A>G	NP_001136243.1:n.*96A>G
NM_001142772.1:c.*96A>G	NP_001136244.1:n.*96A>G
NM_001354420.1:c.*96A>G	NP_001341349.1:n.*96A>G
NM_001354429.1:c.*96A>G	NP_001341358.1:n.*96A>G
XR_001747192.2:n.11611A>G
XR_001747193.2:n.11602A>G
NM_001142771.2:c.*96A>G	NP_001136243.1:n.*96A>G
NM_001142772.2:c.*96A>G	NP_001136244.1:n.*96A>G
NM_001354420.2:c.*96A>G	NP_001341349.1:n.*96A>G
NM_001354429.2:c.*96A>G	NP_001341358.1:n.*96A>G
NM_001384140.1:c.*96A>G MANE Select	NP_001371069.1:n.*96A>G