Canonical Allele Identifier: CA397561699

Gene: PRPF8

Linked Data

• MyVariant Identifiers: chr17:g.1554106A>C (hg19) ; chr17:g.1650812A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1650812A>C , CM000679.2:g.1650812A>C	GRCh38
NC_000017.10:g.1554106A>C , CM000679.1:g.1554106A>C	GRCh37
NC_000017.9:g.1500856A>C	NCBI36
NG_009118.1:g.39071T>G
NG_033061.1:g.4287T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6818T>G	ENSP00000460849.2:p.Leu2273Arg
ENST00000703537.1:c.2746T>G
ENST00000703538.1:c.*6721T>G	ENSP00000515361.1:n.*6721T>G
ENST00000703539.1:n.3312T>G
ENST00000703540.1:c.6851T>G	ENSP00000515362.1:p.Leu2284Arg
ENST00000703541.1:c.6863T>G	ENSP00000515363.1:p.Leu2288Arg
ENST00000304992.11:c.6998T>G MANE Select	ENSP00000304350.6:p.Leu2333Arg
ENST00000304992.10:c.6998T>G	ENSP00000304350.6:p.Leu2333Arg
ENST00000571958.1:c.197T>G
ENST00000572621.5:c.6998T>G	ENSP00000460348.1:p.Leu2333Arg
NM_006445.3:c.6998T>G	NP_006436.3:p.Leu2333Arg
XM_024450537.1:c.6998T>G	XP_024306305.1:p.Leu2333Arg
NM_006445.4:c.6998T>G MANE Select	NP_006436.3:p.Leu2333Arg