Canonical Allele Identifier: CA1910756086

Gene: PCDH15

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806721C= , CM000672.2:g.53806721C=	GRCh38
NC_000010.10:g.55566481C= , CM000672.1:g.55566481C=	GRCh37
NC_000010.9:g.55236487C=	NCBI36
NG_009191.2:g.999571G=
NG_009191.3:g.1827462G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642496.1:c.3940G=
ENST00000644397.2:c.5081G= MANE Select	ENSP00000495195.1:p.Ser1694=
ENST00000373965.6:c.4892G=	ENSP00000363076.3:p.Ser1631=
ENST00000414778.5:c.4889G=	ENSP00000410304.2:p.Ser1630=
ENST00000495484.5:c.1109G=	ENSP00000480780.1:p.Ser370=
ENST00000614895.4:c.4904G=	ENSP00000478512.1:p.Ser1635=
ENST00000616114.4:c.4886G=	ENSP00000483745.1:p.Ser1629=
ENST00000618301.4:c.1241G=	ENSP00000482780.1:p.Ser414=
ENST00000621708.4:c.4907G=	ENSP00000484454.1:p.Ser1636=
NM_001142771.1:c.4907G=	NP_001136243.1:p.Ser1636=
NM_001142772.1:c.4892G=	NP_001136244.1:p.Ser1631=
NM_001354420.1:c.4886G=	NP_001341349.1:p.Ser1629=
NM_001354429.1:c.5015G=	NP_001341358.1:p.Ser1672=
XR_001747192.2:n.11373G=
XR_001747193.2:n.11364G=
NM_001142771.2:c.4907G=	NP_001136243.1:p.Ser1636=
NM_001142772.2:c.4892G=	NP_001136244.1:p.Ser1631=
NM_001354420.2:c.4886G=	NP_001341349.1:p.Ser1629=
NM_001354429.2:c.5015G=	NP_001341358.1:p.Ser1672=
NM_001384140.1:c.5081G= MANE Select	NP_001371069.1:p.Ser1694=