Canonical Allele Identifier: CA2242977358

Gene: PRPF8

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1650895G= , CM000679.2:g.1650895G=	GRCh38
NC_000017.10:g.1554189G= , CM000679.1:g.1554189G=	GRCh37
NC_000017.9:g.1500939G=	NCBI36
NG_009118.1:g.38988C=
NG_033061.1:g.4204C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6735C=	ENSP00000460849.2:p.Tyr2245=
ENST00000703537.1:c.2663C=
ENST00000703538.1:c.*6638C=	ENSP00000515361.1:n.*6638C=
ENST00000703539.1:n.3229C=
ENST00000703540.1:c.6768C=	ENSP00000515362.1:p.Tyr2256=
ENST00000703541.1:c.6780C=	ENSP00000515363.1:p.Tyr2260=
ENST00000304992.11:c.6915C= MANE Select	ENSP00000304350.6:p.Tyr2305=
ENST00000304992.10:c.6915C=	ENSP00000304350.6:p.Tyr2305=
ENST00000571958.1:c.163-49C=
ENST00000572621.5:c.6915C=	ENSP00000460348.1:p.Tyr2305=
ENST00000572723.1:n.904C=
NM_006445.3:c.6915C=	NP_006436.3:p.Tyr2305=
XM_024450537.1:c.6915C=	XP_024306305.1:p.Tyr2305=
NM_006445.4:c.6915C= MANE Select	NP_006436.3:p.Tyr2305=