Canonical Allele Identifier: CA2242977280
Gene: PRPF8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1650851A= , CM000679.2:g.1650851A= GRCh38
NC_000017.10:g.1554145A= , CM000679.1:g.1554145A= GRCh37
NC_000017.9:g.1500895A= NCBI36
NG_009118.1:g.39032T=
NG_033061.1:g.4248T=

Transcript Alleles

HGVS Amino-acid change
ENST00000573725.2:c.6779T= ENSP00000460849.2:p.Leu2260=
ENST00000703537.1:c.2707T=
ENST00000703538.1:c.*6682T= ENSP00000515361.1:n.*6682T=
ENST00000703539.1:n.3273T=
ENST00000703540.1:c.6812T= ENSP00000515362.1:p.Leu2271=
ENST00000703541.1:c.6824T= ENSP00000515363.1:p.Leu2275=
ENST00000304992.11:c.6959T= MANE Select ENSP00000304350.6:p.Leu2320=
ENST00000304992.10:c.6959T= ENSP00000304350.6:p.Leu2320=
ENST00000571958.1:c.163-5T=
ENST00000572621.5:c.6959T= ENSP00000460348.1:p.Leu2320=
ENST00000572723.1:n.948T=
NM_006445.3:c.6959T= NP_006436.3:p.Leu2320=
XM_024450537.1:c.6959T= XP_024306305.1:p.Leu2320=
NM_006445.4:c.6959T= MANE Select NP_006436.3:p.Leu2320=