Canonical Allele Identifier: CA2808190794

Gene: PRPF8

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1650735T>G , CM000679.2:g.1650735T>G	GRCh38
NC_000017.10:g.1554029T>G , CM000679.1:g.1554029T>G	GRCh37
NC_000017.9:g.1500779T>G	NCBI36
NG_009118.1:g.39148A>C
NG_033061.1:g.4364A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.*67A>C	ENSP00000460849.2:n.*67A>C
ENST00000703537.1:c.2823A>C
ENST00000703538.1:c.*6798A>C	ENSP00000515361.1:n.*6798A>C
ENST00000703539.1:n.3389A>C
ENST00000703540.1:c.*67A>C	ENSP00000515362.1:n.*67A>C
ENST00000304992.11:c.*67A>C MANE Select	ENSP00000304350.6:n.*67A>C
ENST00000304992.10:c.*67A>C	ENSP00000304350.6:n.*67A>C
ENST00000571958.1:c.274A>C
ENST00000572621.5:c.*67A>C	ENSP00000460348.1:n.*67A>C
NM_006445.3:c.*67A>C	NP_006436.3:n.*67A>C
XM_024450537.1:c.*67A>C	XP_024306305.1:n.*67A>C
NM_006445.4:c.*67A>C MANE Select	NP_006436.3:n.*67A>C