Canonical Allele Identifier: CA2242977247

Gene: PRPF8

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1650837C= , CM000679.2:g.1650837C=	GRCh38
NC_000017.10:g.1554131C= , CM000679.1:g.1554131C=	GRCh37
NC_000017.9:g.1500881C=	NCBI36
NG_009118.1:g.39046G=
NG_033061.1:g.4262G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6793G=	ENSP00000460849.2:p.Val2265=
ENST00000703537.1:c.2721G=
ENST00000703538.1:c.*6696G=	ENSP00000515361.1:n.*6696G=
ENST00000703539.1:n.3287G=
ENST00000703540.1:c.6826G=	ENSP00000515362.1:p.Val2276=
ENST00000703541.1:c.6838G=	ENSP00000515363.1:p.Val2280=
ENST00000304992.11:c.6973G= MANE Select	ENSP00000304350.6:p.Val2325=
ENST00000304992.10:c.6973G=	ENSP00000304350.6:p.Val2325=
ENST00000571958.1:c.172G=
ENST00000572621.5:c.6973G=	ENSP00000460348.1:p.Val2325=
NM_006445.3:c.6973G=	NP_006436.3:p.Val2325=
XM_024450537.1:c.6973G=	XP_024306305.1:p.Val2325=
NM_006445.4:c.6973G= MANE Select	NP_006436.3:p.Val2325=