Canonical Allele Identifier: CA2242977809

Gene: PRPF8

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1651255C= , CM000679.2:g.1651255C=	GRCh38
NC_000017.10:g.1554549C= , CM000679.1:g.1554549C=	GRCh37
NC_000017.9:g.1501299C=	NCBI36
NG_009118.1:g.38628G=
NG_033061.1:g.3844G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6526G=	ENSP00000460849.2:p.Glu2176=
ENST00000703537.1:c.2454G=
ENST00000703538.1:c.*6429G=	ENSP00000515361.1:n.*6429G=
ENST00000703539.1:n.3020G=
ENST00000703540.1:c.6559G=	ENSP00000515362.1:p.Glu2187=
ENST00000703541.1:c.6571G=	ENSP00000515363.1:p.Glu2191=
ENST00000304992.11:c.6706G= MANE Select	ENSP00000304350.6:p.Glu2236=
ENST00000304992.10:c.6706G=	ENSP00000304350.6:p.Glu2236=
ENST00000571958.1:c.15G=
ENST00000572621.5:c.6706G=	ENSP00000460348.1:p.Glu2236=
ENST00000572723.1:n.695G=
NM_006445.3:c.6706G=	NP_006436.3:p.Glu2236=
XM_024450537.1:c.6706G=	XP_024306305.1:p.Glu2236=
NM_006445.4:c.6706G= MANE Select	NP_006436.3:p.Glu2236=