Canonical Allele Identifier: CA1910756266

Gene: PCDH15

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806804T= , CM000672.2:g.53806804T=	GRCh38
NC_000010.10:g.55566564T= , CM000672.1:g.55566564T=	GRCh37
NC_000010.9:g.55236570T=	NCBI36
NG_009191.2:g.999488A=
NG_009191.3:g.1827379A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642496.1:c.3857A=
ENST00000644397.2:c.4998A= MANE Select	ENSP00000495195.1:p.Ala1666=
ENST00000373965.6:c.4809A=	ENSP00000363076.3:p.Ala1603=
ENST00000414778.5:c.4806A=	ENSP00000410304.2:p.Ala1602=
ENST00000495484.5:c.1026A=	ENSP00000480780.1:p.Ala342=
ENST00000614895.4:c.4821A=	ENSP00000478512.1:p.Ala1607=
ENST00000616114.4:c.4803A=	ENSP00000483745.1:p.Ala1601=
ENST00000618301.4:c.1158A=	ENSP00000482780.1:p.Ala386=
ENST00000621708.4:c.4824A=	ENSP00000484454.1:p.Ala1608=
NM_001142771.1:c.4824A=	NP_001136243.1:p.Ala1608=
NM_001142772.1:c.4809A=	NP_001136244.1:p.Ala1603=
NM_001354420.1:c.4803A=	NP_001341349.1:p.Ala1601=
NM_001354429.1:c.4932A=	NP_001341358.1:p.Ala1644=
XR_001747192.2:n.11290A=
XR_001747193.2:n.11281A=
NM_001142771.2:c.4824A=	NP_001136243.1:p.Ala1608=
NM_001142772.2:c.4809A=	NP_001136244.1:p.Ala1603=
NM_001354420.2:c.4803A=	NP_001341349.1:p.Ala1601=
NM_001354429.2:c.4932A=	NP_001341358.1:p.Ala1644=
NM_001384140.1:c.4998A= MANE Select	NP_001371069.1:p.Ala1666=