Canonical Allele Identifier: CA397564175

Gene: PRPF8

Linked Data

• MyVariant Identifiers: chr17:g.1554587C>A (hg19) ; chr17:g.1651293C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1651293C>A , CM000679.2:g.1651293C>A	GRCh38
NC_000017.10:g.1554587C>A , CM000679.1:g.1554587C>A	GRCh37
NC_000017.9:g.1501337C>A	NCBI36
NG_009118.1:g.38590G>T
NG_033061.1:g.3806G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6488G>T	ENSP00000460849.2:p.Cys2163Phe
ENST00000703537.1:c.2416G>T
ENST00000703538.1:c.*6391G>T	ENSP00000515361.1:n.*6391G>T
ENST00000703539.1:n.2982G>T
ENST00000703540.1:c.6521G>T	ENSP00000515362.1:p.Cys2174Phe
ENST00000703541.1:c.6533G>T	ENSP00000515363.1:p.Cys2178Phe
ENST00000304992.11:c.6668G>T MANE Select	ENSP00000304350.6:p.Cys2223Phe
ENST00000304992.10:c.6668G>T	ENSP00000304350.6:p.Cys2223Phe
ENST00000572621.5:c.6668G>T	ENSP00000460348.1:p.Cys2223Phe
ENST00000572723.1:n.657G>T
NM_006445.3:c.6668G>T	NP_006436.3:p.Cys2223Phe
XM_024450537.1:c.6668G>T	XP_024306305.1:p.Cys2223Phe
NM_006445.4:c.6668G>T MANE Select	NP_006436.3:p.Cys2223Phe