Canonical Allele Identifier: CA2242977062
Gene: PRPF8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1650748_1650749delinsTG , CM000679.2:g.1650748_1650749delinsTG GRCh38
NC_000017.10:g.1554042_1554043delinsTG , CM000679.1:g.1554042_1554043delinsTG GRCh37
NC_000017.9:g.1500792_1500793delinsTG NCBI36
NG_009118.1:g.39134_39135delinsCA
NG_033061.1:g.4350_4351delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000573725.2:c.*53_*54delinsCA ENSP00000460849.2:n.*53_*54delinsCA
ENST00000703537.1:c.2809_2810delinsCA
ENST00000703538.1:c.*6784_*6785delinsCA ENSP00000515361.1:n.*6784_*6785delinsCA
ENST00000703539.1:n.3375_3376delinsCA
ENST00000703540.1:c.*53_*54delinsCA ENSP00000515362.1:n.*53_*54delinsCA
ENST00000304992.11:c.*53_*54delinsCA MANE Select ENSP00000304350.6:n.*53_*54delinsCA
ENST00000304992.10:c.*53_*54delinsCA ENSP00000304350.6:n.*53_*54delinsCA
ENST00000571958.1:c.260_261delinsCA
ENST00000572621.5:c.*53_*54delinsCA ENSP00000460348.1:n.*53_*54delinsCA
NM_006445.3:c.*53_*54delinsCA NP_006436.3:n.*53_*54delinsCA
XM_024450537.1:c.*53_*54delinsCA XP_024306305.1:n.*53_*54delinsCA
NM_006445.4:c.*53_*54delinsCA MANE Select NP_006436.3:n.*53_*54delinsCA