Canonical Allele Identifier: CA1910755873

Gene: PCDH15

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806654G= , CM000672.2:g.53806654G=	GRCh38
NC_000010.10:g.55566414G= , CM000672.1:g.55566414G=	GRCh37
NC_000010.9:g.55236420G=	NCBI36
NG_009191.2:g.999638C=
NG_009191.3:g.1827529C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642496.1:c.4007C=
ENST00000644397.2:c.5148C= MANE Select	ENSP00000495195.1:p.Asp1716=
ENST00000373965.6:c.4959C=	ENSP00000363076.3:p.Asp1653=
ENST00000414778.5:c.4956C=	ENSP00000410304.2:p.Asp1652=
ENST00000495484.5:c.1176C=	ENSP00000480780.1:p.Asp392=
ENST00000614895.4:c.4971C=	ENSP00000478512.1:p.Asp1657=
ENST00000616114.4:c.4953C=	ENSP00000483745.1:p.Asp1651=
ENST00000618301.4:c.1308C=	ENSP00000482780.1:p.Asp436=
ENST00000621708.4:c.4974C=	ENSP00000484454.1:p.Asp1658=
NM_001142771.1:c.4974C=	NP_001136243.1:p.Asp1658=
NM_001142772.1:c.4959C=	NP_001136244.1:p.Asp1653=
NM_001354420.1:c.4953C=	NP_001341349.1:p.Asp1651=
NM_001354429.1:c.5082C=	NP_001341358.1:p.Asp1694=
XR_001747192.2:n.11440C=
XR_001747193.2:n.11431C=
NM_001142771.2:c.4974C=	NP_001136243.1:p.Asp1658=
NM_001142772.2:c.4959C=	NP_001136244.1:p.Asp1653=
NM_001354420.2:c.4953C=	NP_001341349.1:p.Asp1651=
NM_001354429.2:c.5082C=	NP_001341358.1:p.Asp1694=
NM_001384140.1:c.5148C= MANE Select	NP_001371069.1:p.Asp1716=