Canonical Allele Identifier: CA397561898

Gene: PRPF8

Linked Data

• MyVariant Identifiers: chr17:g.1554152C>A (hg19) ; chr17:g.1650858C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1650858C>A , CM000679.2:g.1650858C>A	GRCh38
NC_000017.10:g.1554152C>A , CM000679.1:g.1554152C>A	GRCh37
NC_000017.9:g.1500902C>A	NCBI36
NG_009118.1:g.39025G>T
NG_033061.1:g.4241G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000573725.2:c.6772G>T	ENSP00000460849.2:p.Ala2258Ser
ENST00000703537.1:c.2700G>T
ENST00000703538.1:c.*6675G>T	ENSP00000515361.1:n.*6675G>T
ENST00000703539.1:n.3266G>T
ENST00000703540.1:c.6805G>T	ENSP00000515362.1:p.Ala2269Ser
ENST00000703541.1:c.6817G>T	ENSP00000515363.1:p.Ala2273Ser
ENST00000304992.11:c.6952G>T MANE Select	ENSP00000304350.6:p.Ala2318Ser
ENST00000304992.10:c.6952G>T	ENSP00000304350.6:p.Ala2318Ser
ENST00000571958.1:c.163-12G>T
ENST00000572621.5:c.6952G>T	ENSP00000460348.1:p.Ala2318Ser
ENST00000572723.1:n.941G>T
NM_006445.3:c.6952G>T	NP_006436.3:p.Ala2318Ser
XM_024450537.1:c.6952G>T	XP_024306305.1:p.Ala2318Ser
NM_006445.4:c.6952G>T MANE Select	NP_006436.3:p.Ala2318Ser