Canonical Allele Identifier: CA2576113104
Gene: PRPF8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1650759del , CM000679.2:g.1650759del GRCh38
NC_000017.10:g.1554053del , CM000679.1:g.1554053del GRCh37
NC_000017.9:g.1500803del NCBI36
NG_009118.1:g.39124del
NG_033061.1:g.4340del

Transcript Alleles

HGVS Amino-acid change
ENST00000573725.2:c.*43del ENSP00000460849.2:n.*43del
ENST00000703537.1:c.2799del
ENST00000703538.1:c.*6774del ENSP00000515361.1:n.*6774del
ENST00000703539.1:n.3365del
ENST00000703540.1:c.*43del ENSP00000515362.1:n.*43del
ENST00000304992.11:c.*43del MANE Select ENSP00000304350.6:n.*43del
ENST00000304992.10:c.*43del ENSP00000304350.6:n.*43del
ENST00000571958.1:c.250del
ENST00000572621.5:c.*43del ENSP00000460348.1:n.*43del
NM_006445.3:c.*43del NP_006436.3:n.*43del
XM_024450537.1:c.*43del XP_024306305.1:n.*43del
NM_006445.4:c.*43del MANE Select NP_006436.3:n.*43del