Canonical Allele Identifier: CA397562361

Gene: PRPF8

Linked Data

• MyVariant Identifiers: chr17:g.1554220T>A (hg19) ; chr17:g.1650926T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1650926T>A , CM000679.2:g.1650926T>A	GRCh38
NC_000017.10:g.1554220T>A , CM000679.1:g.1554220T>A	GRCh37
NC_000017.9:g.1500970T>A	NCBI36
NG_009118.1:g.38957A>T
NG_033061.1:g.4173A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6704A>T	ENSP00000460849.2:p.Glu2235Val
ENST00000703537.1:c.2632A>T
ENST00000703538.1:c.*6607A>T	ENSP00000515361.1:n.*6607A>T
ENST00000703539.1:n.3198A>T
ENST00000703540.1:c.6737A>T	ENSP00000515362.1:p.Glu2246Val
ENST00000703541.1:c.6749A>T	ENSP00000515363.1:p.Glu2250Val
ENST00000304992.11:c.6884A>T MANE Select	ENSP00000304350.6:p.Glu2295Val
ENST00000304992.10:c.6884A>T	ENSP00000304350.6:p.Glu2295Val
ENST00000571958.1:c.163-80A>T
ENST00000572621.5:c.6884A>T	ENSP00000460348.1:p.Glu2295Val
ENST00000572723.1:n.873A>T
NM_006445.3:c.6884A>T	NP_006436.3:p.Glu2295Val
XM_024450537.1:c.6884A>T	XP_024306305.1:p.Glu2295Val
NM_006445.4:c.6884A>T MANE Select	NP_006436.3:p.Glu2295Val