Canonical Allele Identifier: CA1910755048

Gene: PCDH15

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806341A= , CM000672.2:g.53806341A=	GRCh38
NC_000010.10:g.55566101A= , CM000672.1:g.55566101A=	GRCh37
NC_000010.9:g.55236107A=	NCBI36
NG_009191.2:g.999951T=
NG_009191.3:g.1827842T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642496.1:c.4320T=
ENST00000644397.2:c.*238T= MANE Select	ENSP00000495195.1:n.*238T=
ENST00000373965.6:c.*238T=	ENSP00000363076.3:n.*238T=
ENST00000414778.5:c.*238T=	ENSP00000410304.2:n.*238T=
ENST00000495484.5:c.*238T=	ENSP00000480780.1:n.*238T=
ENST00000614895.4:c.*238T=	ENSP00000478512.1:n.*238T=
ENST00000616114.4:c.*238T=	ENSP00000483745.1:n.*238T=
ENST00000621708.4:c.*238T=	ENSP00000484454.1:n.*238T=
NM_001142771.1:c.*238T=	NP_001136243.1:n.*238T=
NM_001142772.1:c.*238T=	NP_001136244.1:n.*238T=
NM_001354420.1:c.*238T=	NP_001341349.1:n.*238T=
NM_001354429.1:c.*238T=	NP_001341358.1:n.*238T=
XR_001747192.2:n.11753T=
XR_001747193.2:n.11744T=
NM_001142771.2:c.*238T=	NP_001136243.1:n.*238T=
NM_001142772.2:c.*238T=	NP_001136244.1:n.*238T=
NM_001354420.2:c.*238T=	NP_001341349.1:n.*238T=
NM_001354429.2:c.*238T=	NP_001341358.1:n.*238T=
NM_001384140.1:c.*238T= MANE Select	NP_001371069.1:n.*238T=