Canonical Allele Identifier: CA397570037

Gene: PRPF8

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1656416C>T , CM000679.2:g.1656416C>T	GRCh38
NC_000017.10:g.1559710C>T , CM000679.1:g.1559710C>T	GRCh37
NC_000017.9:g.1506460C>T	NCBI36
NG_009118.1:g.33467G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.5589G>A	ENSP00000460849.2:p.Trp1863Ter
ENST00000703537.1:c.1517G>A
ENST00000703538.1:c.*5492G>A	ENSP00000515361.1:n.*5492G>A
ENST00000703539.1:n.2083G>A
ENST00000703540.1:c.5622G>A	ENSP00000515362.1:p.Trp1874Ter
ENST00000703541.1:c.5634G>A	ENSP00000515363.1:p.Trp1878Ter
ENST00000304992.11:c.5769G>A MANE Select	ENSP00000304350.6:p.Trp1923Ter
ENST00000304992.10:c.5769G>A	ENSP00000304350.6:p.Trp1923Ter
ENST00000572621.5:c.5769G>A	ENSP00000460348.1:p.Trp1923Ter
NM_006445.3:c.5769G>A	NP_006436.3:p.Trp1923Ter
XM_024450537.1:c.5769G>A	XP_024306305.1:p.Trp1923Ter
NM_006445.4:c.5769G>A MANE Select	NP_006436.3:p.Trp1923Ter