Canonical Allele Identifier: CA919773833
Gene: PRPF8 HGNC NCBI

Linked Data

dbSNP Id: rs1567673396

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1650757_1650768del , CM000679.2:g.1650757_1650768del GRCh38
NC_000017.10:g.1554051_1554062del , CM000679.1:g.1554051_1554062del GRCh37
NC_000017.9:g.1500801_1500812del NCBI36
NG_009118.1:g.39118_39129del
NG_033061.1:g.4334_4345del

Transcript Alleles

HGVS Amino-acid change
ENST00000573725.2:c.*37_*48del ENSP00000460849.2:n.*37_*48del
ENST00000703537.1:c.2793_2804del
ENST00000703538.1:c.*6768_*6779del ENSP00000515361.1:n.*6768_*6779del
ENST00000703539.1:n.3359_3370del
ENST00000703540.1:c.*37_*48del ENSP00000515362.1:n.*37_*48del
ENST00000304992.11:c.*37_*48del MANE Select ENSP00000304350.6:n.*37_*48del
ENST00000304992.10:c.*37_*48del ENSP00000304350.6:n.*37_*48del
ENST00000571958.1:c.244_255del
ENST00000572621.5:c.*37_*48del ENSP00000460348.1:n.*37_*48del
NM_006445.3:c.*37_*48del NP_006436.3:n.*37_*48del
XM_024450537.1:c.*37_*48del XP_024306305.1:n.*37_*48del
NM_006445.4:c.*37_*48del MANE Select NP_006436.3:n.*37_*48del