Canonical Allele Identifier: CA397564188

Gene: PRPF8

Linked Data

• MyVariant Identifiers: chr17:g.1554593C>T (hg19) ; chr17:g.1651299C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1651299C>T , CM000679.2:g.1651299C>T	GRCh38
NC_000017.10:g.1554593C>T , CM000679.1:g.1554593C>T	GRCh37
NC_000017.9:g.1501343C>T	NCBI36
NG_009118.1:g.38584G>A
NG_033061.1:g.3800G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6482G>A	ENSP00000460849.2:p.Gly2161Asp
ENST00000703537.1:c.2410G>A
ENST00000703538.1:c.*6385G>A	ENSP00000515361.1:n.*6385G>A
ENST00000703539.1:n.2976G>A
ENST00000703540.1:c.6515G>A	ENSP00000515362.1:p.Gly2172Asp
ENST00000703541.1:c.6527G>A	ENSP00000515363.1:p.Gly2176Asp
ENST00000304992.11:c.6662G>A MANE Select	ENSP00000304350.6:p.Gly2221Asp
ENST00000304992.10:c.6662G>A	ENSP00000304350.6:p.Gly2221Asp
ENST00000572621.5:c.6662G>A	ENSP00000460348.1:p.Gly2221Asp
ENST00000572723.1:n.651G>A
NM_006445.3:c.6662G>A	NP_006436.3:p.Gly2221Asp
XM_024450537.1:c.6662G>A	XP_024306305.1:p.Gly2221Asp
NM_006445.4:c.6662G>A MANE Select	NP_006436.3:p.Gly2221Asp