Canonical Allele Identifier: CA397564111

Gene: PRPF8

Linked Data

• MyVariant Identifiers: chr17:g.1554556A>T (hg19) ; chr17:g.1651262A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1651262A>T , CM000679.2:g.1651262A>T	GRCh38
NC_000017.10:g.1554556A>T , CM000679.1:g.1554556A>T	GRCh37
NC_000017.9:g.1501306A>T	NCBI36
NG_009118.1:g.38621T>A
NG_033061.1:g.3837T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6519T>A	ENSP00000460849.2:p.Ser2173Arg
ENST00000703537.1:c.2447T>A
ENST00000703538.1:c.*6422T>A	ENSP00000515361.1:n.*6422T>A
ENST00000703539.1:n.3013T>A
ENST00000703540.1:c.6552T>A	ENSP00000515362.1:p.Ser2184Arg
ENST00000703541.1:c.6564T>A	ENSP00000515363.1:p.Ser2188Arg
ENST00000304992.11:c.6699T>A MANE Select	ENSP00000304350.6:p.Ser2233Arg
ENST00000304992.10:c.6699T>A	ENSP00000304350.6:p.Ser2233Arg
ENST00000571958.1:c.8T>A
ENST00000572621.5:c.6699T>A	ENSP00000460348.1:p.Ser2233Arg
ENST00000572723.1:n.688T>A
NM_006445.3:c.6699T>A	NP_006436.3:p.Ser2233Arg
XM_024450537.1:c.6699T>A	XP_024306305.1:p.Ser2233Arg
NM_006445.4:c.6699T>A MANE Select	NP_006436.3:p.Ser2233Arg