Canonical Allele Identifier: CA2242977352

Gene: PRPF8

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1650892G= , CM000679.2:g.1650892G=	GRCh38
NC_000017.10:g.1554186G= , CM000679.1:g.1554186G=	GRCh37
NC_000017.9:g.1500936G=	NCBI36
NG_009118.1:g.38991C=
NG_033061.1:g.4207C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6738C=	ENSP00000460849.2:p.His2246=
ENST00000703537.1:c.2666C=
ENST00000703538.1:c.*6641C=	ENSP00000515361.1:n.*6641C=
ENST00000703539.1:n.3232C=
ENST00000703540.1:c.6771C=	ENSP00000515362.1:p.His2257=
ENST00000703541.1:c.6783C=	ENSP00000515363.1:p.His2261=
ENST00000304992.11:c.6918C= MANE Select	ENSP00000304350.6:p.His2306=
ENST00000304992.10:c.6918C=	ENSP00000304350.6:p.His2306=
ENST00000571958.1:c.163-46C=
ENST00000572621.5:c.6918C=	ENSP00000460348.1:p.His2306=
ENST00000572723.1:n.907C=
NM_006445.3:c.6918C=	NP_006436.3:p.His2306=
XM_024450537.1:c.6918C=	XP_024306305.1:p.His2306=
NM_006445.4:c.6918C= MANE Select	NP_006436.3:p.His2306=