Canonical Allele Identifier: CA1910755863

Gene: PCDH15

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806652T= , CM000672.2:g.53806652T=	GRCh38
NC_000010.10:g.55566412T= , CM000672.1:g.55566412T=	GRCh37
NC_000010.9:g.55236418T=	NCBI36
NG_009191.2:g.999640A=
NG_009191.3:g.1827531A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642496.1:c.4009A=
ENST00000644397.2:c.5150A= MANE Select	ENSP00000495195.1:p.His1717=
ENST00000373965.6:c.4961A=	ENSP00000363076.3:p.His1654=
ENST00000414778.5:c.4958A=	ENSP00000410304.2:p.His1653=
ENST00000495484.5:c.1178A=	ENSP00000480780.1:p.His393=
ENST00000614895.4:c.4973A=	ENSP00000478512.1:p.His1658=
ENST00000616114.4:c.4955A=	ENSP00000483745.1:p.His1652=
ENST00000618301.4:c.1310A=	ENSP00000482780.1:p.His437=
ENST00000621708.4:c.4976A=	ENSP00000484454.1:p.His1659=
NM_001142771.1:c.4976A=	NP_001136243.1:p.His1659=
NM_001142772.1:c.4961A=	NP_001136244.1:p.His1654=
NM_001354420.1:c.4955A=	NP_001341349.1:p.His1652=
NM_001354429.1:c.5084A=	NP_001341358.1:p.His1695=
XR_001747192.2:n.11442A=
XR_001747193.2:n.11433A=
NM_001142771.2:c.4976A=	NP_001136243.1:p.His1659=
NM_001142772.2:c.4961A=	NP_001136244.1:p.His1654=
NM_001354420.2:c.4955A=	NP_001341349.1:p.His1652=
NM_001354429.2:c.5084A=	NP_001341358.1:p.His1695=
NM_001384140.1:c.5150A= MANE Select	NP_001371069.1:p.His1717=