Canonical Allele Identifier: CA2523235974
Gene: PRPF8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1651124_1651125insTGTCGCTGCTTACACCGATAGAGTAAACCTCGCTACCCTTATTGCTATCGAAGATGTAAAGAGTCTGTGGCTCAGTAGTAG , CM000679.2:g.1651124_1651125insTGTCGCTGCTTACACCGATAGAGTAAACCTCGCTACCCTTATTGCTATCGAAGATGTAAAGAGTCTGTGGCTCAGTAGTAG GRCh38
NC_000017.10:g.1554418_1554419insTGTCGCTGCTTACACCGATAGAGTAAACCTCGCTACCCTTATTGCTATCGAAGATGTAAAGAGTCTGTGGCTCAGTAGTAG , CM000679.1:g.1554418_1554419insTGTCGCTGCTTACACCGATAGAGTAAACCTCGCTACCCTTATTGCTATCGAAGATGTAAAGAGTCTGTGGCTCAGTAGTAG GRCh37
NC_000017.9:g.1501168_1501169insTGTCGCTGCTTACACCGATAGAGTAAACCTCGCTACCCTTATTGCTATCGAAGATGTAAAGAGTCTGTGGCTCAGTAGTAG NCBI36
NG_009118.1:g.38758_38759insCTACTACTGAGCCACAGACTCTTTACATCTTCGATAGCAATAAGGGTAGCGAGGTTTACTCTATCGGTGTAAGCAGCGACA
NG_033061.1:g.3974_3975insCTACTACTGAGCCACAGACTCTTTACATCTTCGATAGCAATAAGGGTAGCGAGGTTTACTCTATCGGTGTAAGCAGCGACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000573725.2:c.6656_6657insCTACTACTGAGCCACAGACTCTTTACATCTTCGATAGCAATAAGGGTAGCGAGGTTTACTCTATCGGTGTAAGCAGCGACA ENSP00000460849.2:p.Trp2219CysfsTer4
ENST00000703537.1:c.2584_2585insCTACTACTGAGCCACAGACTCTTTACATCTTCGATAGCAATAAGGGTAGCGAGGTTTACTCTATCGGTGTAAGCAGCGACA
ENST00000703538.1:c.*6559_*6560insCTACTACTGAGCCACAGACTCTTTACATCTTCGATAGCAATAAGGGTAGCGAGGTTTACTCTATCGGTGTAAGCAGCGACA ENSP00000515361.1:n.*6559_*6560insCTACTACTGAGCCACAGACTCTTTACA...
ENST00000703539.1:n.3150_3151insCTACTACTGAGCCACAGACTCTTTACATCTTCGATAGCAATAAGGGTAGCGAGGTTTACTCTATCGGTGTAAGCAGCGACA
ENST00000703540.1:c.6689_6690insCTACTACTGAGCCACAGACTCTTTACATCTTCGATAGCAATAAGGGTAGCGAGGTTTACTCTATCGGTGTAAGCAGCGACA ENSP00000515362.1:p.Trp2230CysfsTer4
ENST00000703541.1:c.6701_6702insCTACTACTGAGCCACAGACTCTTTACATCTTCGATAGCAATAAGGGTAGCGAGGTTTACTCTATCGGTGTAAGCAGCGACA ENSP00000515363.1:p.Trp2234CysfsTer4
ENST00000304992.11:c.6836_6837insCTACTACTGAGCCACAGACTCTTTACATCTTCGATAGCAATAAGGGTAGCGAGGTTTACTCTATCGGTGTAAGCAGCGACA MANE Select ENSP00000304350.6:p.Trp2279CysfsTer4
ENST00000304992.10:c.6836_6837insCTACTACTGAGCCACAGACTCTTTACATCTTCGATAGCAATAAGGGTAGCGAGGTTTACTCTATCGGTGTAAGCAGCGACA ENSP00000304350.6:p.Trp2279CysfsTer4
ENST00000571958.1:c.145_146insCTACTACTGAGCCACAGACTCTTTACATCTTCGATAGCAATAAGGGTAGCGAGGTTTACTCTATCGGTGTAAGCAGCGACA
ENST00000572621.5:c.6836_6837insCTACTACTGAGCCACAGACTCTTTACATCTTCGATAGCAATAAGGGTAGCGAGGTTTACTCTATCGGTGTAAGCAGCGACA ENSP00000460348.1:p.Trp2279CysfsTer4
ENST00000572723.1:n.825_826insCTACTACTGAGCCACAGACTCTTTACATCTTCGATAGCAATAAGGGTAGCGAGGTTTACTCTATCGGTGTAAGCAGCGACA
NM_006445.3:c.6836_6837insCTACTACTGAGCCACAGACTCTTTACATCTTCGATAGCAATAAGGGTAGCGAGGTTTACTCTATCGGTGTAAGCAGCGACA NP_006436.3:p.Trp2279CysfsTer4
XM_024450537.1:c.6836_6837insCTACTACTGAGCCACAGACTCTTTACATCTTCGATAGCAATAAGGGTAGCGAGGTTTACTCTATCGGTGTAAGCAGCGACA XP_024306305.1:p.Trp2279CysfsTer4
NM_006445.4:c.6836_6837insCTACTACTGAGCCACAGACTCTTTACATCTTCGATAGCAATAAGGGTAGCGAGGTTTACTCTATCGGTGTAAGCAGCGACA MANE Select NP_006436.3:p.Trp2279CysfsTer4