Canonical Allele Identifier: CA2242977285
Gene: PRPF8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1650855G= , CM000679.2:g.1650855G= GRCh38
NC_000017.10:g.1554149G= , CM000679.1:g.1554149G= GRCh37
NC_000017.9:g.1500899G= NCBI36
NG_009118.1:g.39028C=
NG_033061.1:g.4244C=

Transcript Alleles

HGVS Amino-acid change
ENST00000573725.2:c.6775C= ENSP00000460849.2:p.Leu2259=
ENST00000703537.1:c.2703C=
ENST00000703538.1:c.*6678C= ENSP00000515361.1:n.*6678C=
ENST00000703539.1:n.3269C=
ENST00000703540.1:c.6808C= ENSP00000515362.1:p.Leu2270=
ENST00000703541.1:c.6820C= ENSP00000515363.1:p.Leu2274=
ENST00000304992.11:c.6955C= MANE Select ENSP00000304350.6:p.Leu2319=
ENST00000304992.10:c.6955C= ENSP00000304350.6:p.Leu2319=
ENST00000571958.1:c.163-9C=
ENST00000572621.5:c.6955C= ENSP00000460348.1:p.Leu2319=
ENST00000572723.1:n.944C=
NM_006445.3:c.6955C= NP_006436.3:p.Leu2319=
XM_024450537.1:c.6955C= XP_024306305.1:p.Leu2319=
NM_006445.4:c.6955C= MANE Select NP_006436.3:p.Leu2319=