Canonical Allele Identifier: CA2242977300

Gene: PRPF8

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1650864T= , CM000679.2:g.1650864T=	GRCh38
NC_000017.10:g.1554158T= , CM000679.1:g.1554158T=	GRCh37
NC_000017.9:g.1500908T=	NCBI36
NG_009118.1:g.39019A=
NG_033061.1:g.4235A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6766A=	ENSP00000460849.2:p.Asn2256=
ENST00000703537.1:c.2694A=
ENST00000703538.1:c.*6669A=	ENSP00000515361.1:n.*6669A=
ENST00000703539.1:n.3260A=
ENST00000703540.1:c.6799A=	ENSP00000515362.1:p.Asn2267=
ENST00000703541.1:c.6811A=	ENSP00000515363.1:p.Asn2271=
ENST00000304992.11:c.6946A= MANE Select	ENSP00000304350.6:p.Asn2316=
ENST00000304992.10:c.6946A=	ENSP00000304350.6:p.Asn2316=
ENST00000571958.1:c.163-18A=
ENST00000572621.5:c.6946A=	ENSP00000460348.1:p.Asn2316=
ENST00000572723.1:n.935A=
NM_006445.3:c.6946A=	NP_006436.3:p.Asn2316=
XM_024450537.1:c.6946A=	XP_024306305.1:p.Asn2316=
NM_006445.4:c.6946A= MANE Select	NP_006436.3:p.Asn2316=