Canonical Allele Identifier: CA1910755828

Gene: PCDH15

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806635C= , CM000672.2:g.53806635C=	GRCh38
NC_000010.10:g.55566395C= , CM000672.1:g.55566395C=	GRCh37
NC_000010.9:g.55236401C=	NCBI36
NG_009191.2:g.999657G=
NG_009191.3:g.1827548G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642496.1:c.4026G=
ENST00000644397.2:c.5167G= MANE Select	ENSP00000495195.1:p.Glu1723=
ENST00000373965.6:c.4978G=	ENSP00000363076.3:p.Glu1660=
ENST00000414778.5:c.4975G=	ENSP00000410304.2:p.Glu1659=
ENST00000495484.5:c.1195G=	ENSP00000480780.1:p.Glu399=
ENST00000614895.4:c.4990G=	ENSP00000478512.1:p.Glu1664=
ENST00000616114.4:c.4972G=	ENSP00000483745.1:p.Glu1658=
ENST00000618301.4:c.1327G=	ENSP00000482780.1:p.Glu443=
ENST00000621708.4:c.4993G=	ENSP00000484454.1:p.Glu1665=
NM_001142771.1:c.4993G=	NP_001136243.1:p.Glu1665=
NM_001142772.1:c.4978G=	NP_001136244.1:p.Glu1660=
NM_001354420.1:c.4972G=	NP_001341349.1:p.Glu1658=
NM_001354429.1:c.5101G=	NP_001341358.1:p.Glu1701=
XR_001747192.2:n.11459G=
XR_001747193.2:n.11450G=
NM_001142771.2:c.4993G=	NP_001136243.1:p.Glu1665=
NM_001142772.2:c.4978G=	NP_001136244.1:p.Glu1660=
NM_001354420.2:c.4972G=	NP_001341349.1:p.Glu1658=
NM_001354429.2:c.5101G=	NP_001341358.1:p.Glu1701=
NM_001384140.1:c.5167G= MANE Select	NP_001371069.1:p.Glu1723=