Canonical Allele Identifier: CA2788034356

Gene: PCDH15

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806279_53806280insAGA , CM000672.2:g.53806279_53806280insAGA	GRCh38
NC_000010.10:g.55566039_55566040insAGA , CM000672.1:g.55566039_55566040insAGA	GRCh37
NC_000010.9:g.55236045_55236046insAGA	NCBI36
NG_009191.2:g.1000012_1000013insTCT
NG_009191.3:g.1827903_1827904insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644397.2:c.*299_*300insTCT MANE Select	ENSP00000495195.1:n.*299_*300insTCT
ENST00000373965.6:c.*299_*300insTCT	ENSP00000363076.3:n.*299_*300insTCT
ENST00000414778.5:c.*299_*300insTCT	ENSP00000410304.2:n.*299_*300insTCT
ENST00000614895.4:c.*299_*300insTCT	ENSP00000478512.1:n.*299_*300insTCT
ENST00000616114.4:c.*299_*300insTCT	ENSP00000483745.1:n.*299_*300insTCT
NM_001142771.1:c.*299_*300insTCT	NP_001136243.1:n.*299_*300insTCT
NM_001142772.1:c.*299_*300insTCT	NP_001136244.1:n.*299_*300insTCT
NM_001354420.1:c.*299_*300insTCT	NP_001341349.1:n.*299_*300insTCT
NM_001354429.1:c.*299_*300insTCT	NP_001341358.1:n.*299_*300insTCT
XR_001747192.2:n.11814_11815insTCT
XR_001747193.2:n.11805_11806insTCT
NM_001142771.2:c.*299_*300insTCT	NP_001136243.1:n.*299_*300insTCT
NM_001142772.2:c.*299_*300insTCT	NP_001136244.1:n.*299_*300insTCT
NM_001354420.2:c.*299_*300insTCT	NP_001341349.1:n.*299_*300insTCT
NM_001354429.2:c.*299_*300insTCT	NP_001341358.1:n.*299_*300insTCT
NM_001384140.1:c.*299_*300insTCT MANE Select	NP_001371069.1:n.*299_*300insTCT