Canonical Allele Identifier: CA397564151

Gene: PRPF8

Linked Data

• dbSNP Id: rs1911041737
• MyVariant Identifiers: chr17:g.1554575G>A (hg19) ; chr17:g.1651281G>A (hg38)
• PubMed: PMID:25363768

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1651281G>A , CM000679.2:g.1651281G>A	GRCh38
NC_000017.10:g.1554575G>A , CM000679.1:g.1554575G>A	GRCh37
NC_000017.9:g.1501325G>A	NCBI36
NG_009118.1:g.38602C>T
NG_033061.1:g.3818C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6500C>T	ENSP00000460849.2:p.Ala2167Val
ENST00000703537.1:c.2428C>T
ENST00000703538.1:c.*6403C>T	ENSP00000515361.1:n.*6403C>T
ENST00000703539.1:n.2994C>T
ENST00000703540.1:c.6533C>T	ENSP00000515362.1:p.Ala2178Val
ENST00000703541.1:c.6545C>T	ENSP00000515363.1:p.Ala2182Val
ENST00000304992.11:c.6680C>T MANE Select	ENSP00000304350.6:p.Ala2227Val
ENST00000304992.10:c.6680C>T	ENSP00000304350.6:p.Ala2227Val
ENST00000572621.5:c.6680C>T	ENSP00000460348.1:p.Ala2227Val
ENST00000572723.1:n.669C>T
NM_006445.3:c.6680C>T	NP_006436.3:p.Ala2227Val
XM_024450537.1:c.6680C>T	XP_024306305.1:p.Ala2227Val
NM_006445.4:c.6680C>T MANE Select	NP_006436.3:p.Ala2227Val