Canonical Allele Identifier: CA2609218088

Gene: PCDH15

Linked Data

• gnomAD v4: 10-53806171-C-CTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806174_53806177dup , CM000672.2:g.53806174_53806177dup	GRCh38
NC_000010.10:g.55565934_55565937dup , CM000672.1:g.55565934_55565937dup	GRCh37
NC_000010.9:g.55235940_55235943dup	NCBI36
NG_009191.2:g.1000117_1000120dup
NG_009191.3:g.1828008_1828011dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644397.2:c.*404_*407dup MANE Select	ENSP00000495195.1:n.*404_*407dup
ENST00000373965.6:c.*404_*407dup	ENSP00000363076.3:n.*404_*407dup
ENST00000414778.5:c.*404_*407dup	ENSP00000410304.2:n.*404_*407dup
ENST00000614895.4:c.*404_*407dup	ENSP00000478512.1:n.*404_*407dup
ENST00000616114.4:c.*404_*407dup	ENSP00000483745.1:n.*404_*407dup
NM_001142771.1:c.*404_*407dup	NP_001136243.1:n.*404_*407dup
NM_001142772.1:c.*404_*407dup	NP_001136244.1:n.*404_*407dup
NM_001354420.1:c.*404_*407dup	NP_001341349.1:n.*404_*407dup
NM_001354429.1:c.*404_*407dup	NP_001341358.1:n.*404_*407dup
XR_001747192.2:n.11919_11922dup
XR_001747193.2:n.11910_11913dup
NM_001142771.2:c.*404_*407dup	NP_001136243.1:n.*404_*407dup
NM_001142772.2:c.*404_*407dup	NP_001136244.1:n.*404_*407dup
NM_001354420.2:c.*404_*407dup	NP_001341349.1:n.*404_*407dup
NM_001354429.2:c.*404_*407dup	NP_001341358.1:n.*404_*407dup
NM_001384140.1:c.*404_*407dup MANE Select	NP_001371069.1:n.*404_*407dup