Canonical Allele Identifier: CA2242977229

Gene: PRPF8

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1650827G= , CM000679.2:g.1650827G=	GRCh38
NC_000017.10:g.1554121G= , CM000679.1:g.1554121G=	GRCh37
NC_000017.9:g.1500871G=	NCBI36
NG_009118.1:g.39056C=
NG_033061.1:g.4272C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6803C=	ENSP00000460849.2:p.Ala2268=
ENST00000703537.1:c.2731C=
ENST00000703538.1:c.*6706C=	ENSP00000515361.1:n.*6706C=
ENST00000703539.1:n.3297C=
ENST00000703540.1:c.6836C=	ENSP00000515362.1:p.Ala2279=
ENST00000703541.1:c.6848C=	ENSP00000515363.1:p.Ala2283=
ENST00000304992.11:c.6983C= MANE Select	ENSP00000304350.6:p.Ala2328=
ENST00000304992.10:c.6983C=	ENSP00000304350.6:p.Ala2328=
ENST00000571958.1:c.182C=
ENST00000572621.5:c.6983C=	ENSP00000460348.1:p.Ala2328=
NM_006445.3:c.6983C=	NP_006436.3:p.Ala2328=
XM_024450537.1:c.6983C=	XP_024306305.1:p.Ala2328=
NM_006445.4:c.6983C= MANE Select	NP_006436.3:p.Ala2328=