Canonical Allele Identifier: CA8271053
Gene: PRPF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1095157
ClinVar RCV Id: RCV001415943
dbSNP Id: rs375319645
gnomAD v2: 17-1554207-C-T
gnomAD v3: 17-1650913-C-T
gnomAD v4: 17-1650913-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1650913C>T , CM000679.2:g.1650913C>T GRCh38
NC_000017.10:g.1554207C>T , CM000679.1:g.1554207C>T GRCh37
NC_000017.9:g.1500957C>T NCBI36
NG_009118.1:g.38970G>A
NG_033061.1:g.4186G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000573725.2:c.6717G>A ENSP00000460849.2:p.Ala2239=
ENST00000703537.1:c.2645G>A
ENST00000703538.1:c.*6620G>A ENSP00000515361.1:n.*6620G>A
ENST00000703539.1:n.3211G>A
ENST00000703540.1:c.6750G>A ENSP00000515362.1:p.Ala2250=
ENST00000703541.1:c.6762G>A ENSP00000515363.1:p.Ala2254=
ENST00000304992.11:c.6897G>A MANE Select ENSP00000304350.6:p.Ala2299=
ENST00000304992.10:c.6897G>A ENSP00000304350.6:p.Ala2299=
ENST00000571958.1:c.163-67G>A
ENST00000572621.5:c.6897G>A ENSP00000460348.1:p.Ala2299=
ENST00000572723.1:n.886G>A
NM_006445.3:c.6897G>A NP_006436.3:p.Ala2299=
XM_024450537.1:c.6897G>A XP_024306305.1:p.Ala2299=
NM_006445.4:c.6897G>A MANE Select NP_006436.3:p.Ala2299=