Canonical Allele Identifier: CA1910756155

Gene: PCDH15

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806737T= , CM000672.2:g.53806737T=	GRCh38
NC_000010.10:g.55566497T= , CM000672.1:g.55566497T=	GRCh37
NC_000010.9:g.55236503T=	NCBI36
NG_009191.2:g.999555A=
NG_009191.3:g.1827446A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642496.1:c.3924A=
ENST00000644397.2:c.5065A= MANE Select	ENSP00000495195.1:p.Arg1689=
ENST00000373965.6:c.4876A=	ENSP00000363076.3:p.Arg1626=
ENST00000414778.5:c.4873A=	ENSP00000410304.2:p.Arg1625=
ENST00000495484.5:c.1093A=	ENSP00000480780.1:p.Arg365=
ENST00000614895.4:c.4888A=	ENSP00000478512.1:p.Arg1630=
ENST00000616114.4:c.4870A=	ENSP00000483745.1:p.Arg1624=
ENST00000618301.4:c.1225A=	ENSP00000482780.1:p.Arg409=
ENST00000621708.4:c.4891A=	ENSP00000484454.1:p.Arg1631=
NM_001142771.1:c.4891A=	NP_001136243.1:p.Arg1631=
NM_001142772.1:c.4876A=	NP_001136244.1:p.Arg1626=
NM_001354420.1:c.4870A=	NP_001341349.1:p.Arg1624=
NM_001354429.1:c.4999A=	NP_001341358.1:p.Arg1667=
XR_001747192.2:n.11357A=
XR_001747193.2:n.11348A=
NM_001142771.2:c.4891A=	NP_001136243.1:p.Arg1631=
NM_001142772.2:c.4876A=	NP_001136244.1:p.Arg1626=
NM_001354420.2:c.4870A=	NP_001341349.1:p.Arg1624=
NM_001354429.2:c.4999A=	NP_001341358.1:p.Arg1667=
NM_001384140.1:c.5065A= MANE Select	NP_001371069.1:p.Arg1689=