Canonical Allele Identifier: CA1910755754

Gene: PCDH15

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806606G= , CM000672.2:g.53806606G=	GRCh38
NC_000010.10:g.55566366G= , CM000672.1:g.55566366G=	GRCh37
NC_000010.9:g.55236372G=	NCBI36
NG_009191.2:g.999686C=
NG_009191.3:g.1827577C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642496.1:c.4055C=
ENST00000644397.2:c.5196C= MANE Select	ENSP00000495195.1:p.Asn1732=
ENST00000373965.6:c.5007C=	ENSP00000363076.3:p.Asn1669=
ENST00000414778.5:c.5004C=	ENSP00000410304.2:p.Asn1668=
ENST00000495484.5:c.1224C=	ENSP00000480780.1:p.Asn408=
ENST00000614895.4:c.5019C=	ENSP00000478512.1:p.Asn1673=
ENST00000616114.4:c.5001C=	ENSP00000483745.1:p.Asn1667=
ENST00000618301.4:c.1356C=	ENSP00000482780.1:p.Asn452=
ENST00000621708.4:c.5022C=	ENSP00000484454.1:p.Asn1674=
NM_001142771.1:c.5022C=	NP_001136243.1:p.Asn1674=
NM_001142772.1:c.5007C=	NP_001136244.1:p.Asn1669=
NM_001354420.1:c.5001C=	NP_001341349.1:p.Asn1667=
NM_001354429.1:c.5130C=	NP_001341358.1:p.Asn1710=
XR_001747192.2:n.11488C=
XR_001747193.2:n.11479C=
NM_001142771.2:c.5022C=	NP_001136243.1:p.Asn1674=
NM_001142772.2:c.5007C=	NP_001136244.1:p.Asn1669=
NM_001354420.2:c.5001C=	NP_001341349.1:p.Asn1667=
NM_001354429.2:c.5130C=	NP_001341358.1:p.Asn1710=
NM_001384140.1:c.5196C= MANE Select	NP_001371069.1:p.Asn1732=