Canonical Allele Identifier: CA1910755878

Gene: PCDH15

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806657A= , CM000672.2:g.53806657A=	GRCh38
NC_000010.10:g.55566417A= , CM000672.1:g.55566417A=	GRCh37
NC_000010.9:g.55236423A=	NCBI36
NG_009191.2:g.999635T=
NG_009191.3:g.1827526T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642496.1:c.4004T=
ENST00000644397.2:c.5145T= MANE Select	ENSP00000495195.1:p.Ser1715=
ENST00000373965.6:c.4956T=	ENSP00000363076.3:p.Ser1652=
ENST00000414778.5:c.4953T=	ENSP00000410304.2:p.Ser1651=
ENST00000495484.5:c.1173T=	ENSP00000480780.1:p.Ser391=
ENST00000614895.4:c.4968T=	ENSP00000478512.1:p.Ser1656=
ENST00000616114.4:c.4950T=	ENSP00000483745.1:p.Ser1650=
ENST00000618301.4:c.1305T=	ENSP00000482780.1:p.Ser435=
ENST00000621708.4:c.4971T=	ENSP00000484454.1:p.Ser1657=
NM_001142771.1:c.4971T=	NP_001136243.1:p.Ser1657=
NM_001142772.1:c.4956T=	NP_001136244.1:p.Ser1652=
NM_001354420.1:c.4950T=	NP_001341349.1:p.Ser1650=
NM_001354429.1:c.5079T=	NP_001341358.1:p.Ser1693=
XR_001747192.2:n.11437T=
XR_001747193.2:n.11428T=
NM_001142771.2:c.4971T=	NP_001136243.1:p.Ser1657=
NM_001142772.2:c.4956T=	NP_001136244.1:p.Ser1652=
NM_001354420.2:c.4950T=	NP_001341349.1:p.Ser1650=
NM_001354429.2:c.5079T=	NP_001341358.1:p.Ser1693=
NM_001384140.1:c.5145T= MANE Select	NP_001371069.1:p.Ser1715=