Canonical Allele Identifier: CA2808190793
Gene: PRPF8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1650719G>A , CM000679.2:g.1650719G>A GRCh38
NC_000017.10:g.1554013G>A , CM000679.1:g.1554013G>A GRCh37
NC_000017.9:g.1500763G>A NCBI36
NG_009118.1:g.39164C>T
NG_033061.1:g.4380C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000573725.2:c.*83C>T ENSP00000460849.2:n.*83C>T
ENST00000703537.1:c.2839C>T
ENST00000703538.1:c.*6814C>T ENSP00000515361.1:n.*6814C>T
ENST00000703539.1:n.3405C>T
ENST00000703540.1:c.*83C>T ENSP00000515362.1:n.*83C>T
ENST00000304992.11:c.*83C>T MANE Select ENSP00000304350.6:n.*83C>T
ENST00000304992.10:c.*83C>T ENSP00000304350.6:n.*83C>T
ENST00000571958.1:c.290C>T
ENST00000572621.5:c.*83C>T ENSP00000460348.1:n.*83C>T
NM_006445.3:c.*83C>T NP_006436.3:n.*83C>T
XM_024450537.1:c.*83C>T XP_024306305.1:n.*83C>T
NM_006445.4:c.*83C>T MANE Select NP_006436.3:n.*83C>T