Canonical Allele Identifier: CA980683829
Gene: PRPF8 HGNC NCBI

Linked Data

dbSNP Id: rs1910985379

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1650750del , CM000679.2:g.1650750del GRCh38
NC_000017.10:g.1554044del , CM000679.1:g.1554044del GRCh37
NC_000017.9:g.1500794del NCBI36
NG_009118.1:g.39134del
NG_033061.1:g.4350del

Transcript Alleles

HGVS Amino-acid change
ENST00000573725.2:c.*53del ENSP00000460849.2:n.*53del
ENST00000703537.1:c.2809del
ENST00000703538.1:c.*6784del ENSP00000515361.1:n.*6784del
ENST00000703539.1:n.3375del
ENST00000703540.1:c.*53del ENSP00000515362.1:n.*53del
ENST00000304992.11:c.*53del MANE Select ENSP00000304350.6:n.*53del
ENST00000304992.10:c.*53del ENSP00000304350.6:n.*53del
ENST00000571958.1:c.260del
ENST00000572621.5:c.*53del ENSP00000460348.1:n.*53del
NM_006445.3:c.*53del NP_006436.3:n.*53del
XM_024450537.1:c.*53del XP_024306305.1:n.*53del
NM_006445.4:c.*53del MANE Select NP_006436.3:n.*53del