Canonical Allele Identifier: CA2242977287
Gene: PRPF8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1650856A= , CM000679.2:g.1650856A= GRCh38
NC_000017.10:g.1554150A= , CM000679.1:g.1554150A= GRCh37
NC_000017.9:g.1500900A= NCBI36
NG_009118.1:g.39027T=
NG_033061.1:g.4243T=

Transcript Alleles

HGVS Amino-acid change
ENST00000573725.2:c.6774T= ENSP00000460849.2:p.Ala2258=
ENST00000703537.1:c.2702T=
ENST00000703538.1:c.*6677T= ENSP00000515361.1:n.*6677T=
ENST00000703539.1:n.3268T=
ENST00000703540.1:c.6807T= ENSP00000515362.1:p.Ala2269=
ENST00000703541.1:c.6819T= ENSP00000515363.1:p.Ala2273=
ENST00000304992.11:c.6954T= MANE Select ENSP00000304350.6:p.Ala2318=
ENST00000304992.10:c.6954T= ENSP00000304350.6:p.Ala2318=
ENST00000571958.1:c.163-10T=
ENST00000572621.5:c.6954T= ENSP00000460348.1:p.Ala2318=
ENST00000572723.1:n.943T=
NM_006445.3:c.6954T= NP_006436.3:p.Ala2318=
XM_024450537.1:c.6954T= XP_024306305.1:p.Ala2318=
NM_006445.4:c.6954T= MANE Select NP_006436.3:p.Ala2318=