Canonical Allele Identifier: CA2788034293

Gene: PCDH15

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806210del , CM000672.2:g.53806210del	GRCh38
NC_000010.10:g.55565970del , CM000672.1:g.55565970del	GRCh37
NC_000010.9:g.55235976del	NCBI36
NG_009191.2:g.1000082del
NG_009191.3:g.1827973del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644397.2:c.*369del MANE Select	ENSP00000495195.1:n.*369del
ENST00000373965.6:c.*369del	ENSP00000363076.3:n.*369del
ENST00000414778.5:c.*369del	ENSP00000410304.2:n.*369del
ENST00000614895.4:c.*369del	ENSP00000478512.1:n.*369del
ENST00000616114.4:c.*369del	ENSP00000483745.1:n.*369del
NM_001142771.1:c.*369del	NP_001136243.1:n.*369del
NM_001142772.1:c.*369del	NP_001136244.1:n.*369del
NM_001354420.1:c.*369del	NP_001341349.1:n.*369del
NM_001354429.1:c.*369del	NP_001341358.1:n.*369del
XR_001747192.2:n.11884del
XR_001747193.2:n.11875del
NM_001142771.2:c.*369del	NP_001136243.1:n.*369del
NM_001142772.2:c.*369del	NP_001136244.1:n.*369del
NM_001354420.2:c.*369del	NP_001341349.1:n.*369del
NM_001354429.2:c.*369del	NP_001341358.1:n.*369del
NM_001384140.1:c.*369del MANE Select	NP_001371069.1:n.*369del