Canonical Allele Identifier: CA397564211

Gene: PRPF8

Linked Data

• MyVariant Identifiers: chr17:g.1554603A>T (hg19) ; chr17:g.1651309A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1651309A>T , CM000679.2:g.1651309A>T	GRCh38
NC_000017.10:g.1554603A>T , CM000679.1:g.1554603A>T	GRCh37
NC_000017.9:g.1501353A>T	NCBI36
NG_009118.1:g.38574T>A
NG_033061.1:g.3790T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6472T>A	ENSP00000460849.2:p.Phe2158Ile
ENST00000703537.1:c.2400T>A
ENST00000703538.1:c.*6375T>A	ENSP00000515361.1:n.*6375T>A
ENST00000703539.1:n.2966T>A
ENST00000703540.1:c.6505T>A	ENSP00000515362.1:p.Phe2169Ile
ENST00000703541.1:c.6517T>A	ENSP00000515363.1:p.Phe2173Ile
ENST00000304992.11:c.6652T>A MANE Select	ENSP00000304350.6:p.Phe2218Ile
ENST00000304992.10:c.6652T>A	ENSP00000304350.6:p.Phe2218Ile
ENST00000572621.5:c.6652T>A	ENSP00000460348.1:p.Phe2218Ile
ENST00000572723.1:n.641T>A
NM_006445.3:c.6652T>A	NP_006436.3:p.Phe2218Ile
XM_024450537.1:c.6652T>A	XP_024306305.1:p.Phe2218Ile
NM_006445.4:c.6652T>A MANE Select	NP_006436.3:p.Phe2218Ile