Canonical Allele Identifier: CA2242977705

Gene: PRPF8

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1651165G= , CM000679.2:g.1651165G=	GRCh38
NC_000017.10:g.1554459G= , CM000679.1:g.1554459G=	GRCh37
NC_000017.9:g.1501209G=	NCBI36
NG_009118.1:g.38718C=
NG_033061.1:g.3934C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6616C=	ENSP00000460849.2:p.Arg2206=
ENST00000703537.1:c.2544C=
ENST00000703538.1:c.*6519C=	ENSP00000515361.1:n.*6519C=
ENST00000703539.1:n.3110C=
ENST00000703540.1:c.6649C=	ENSP00000515362.1:p.Arg2217=
ENST00000703541.1:c.6661C=	ENSP00000515363.1:p.Arg2221=
ENST00000304992.11:c.6796C= MANE Select	ENSP00000304350.6:p.Arg2266=
ENST00000304992.10:c.6796C=	ENSP00000304350.6:p.Arg2266=
ENST00000571958.1:c.105C=
ENST00000572621.5:c.6796C=	ENSP00000460348.1:p.Arg2266=
ENST00000572723.1:n.785C=
NM_006445.3:c.6796C=	NP_006436.3:p.Arg2266=
XM_024450537.1:c.6796C=	XP_024306305.1:p.Arg2266=
NM_006445.4:c.6796C= MANE Select	NP_006436.3:p.Arg2266=