Canonical Allele Identifier: CA397562140
Gene: PRPF8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1650897A>C , CM000679.2:g.1650897A>C GRCh38
NC_000017.10:g.1554191A>C , CM000679.1:g.1554191A>C GRCh37
NC_000017.9:g.1500941A>C NCBI36
NG_009118.1:g.38986T>G
NG_033061.1:g.4202T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000573725.2:c.6733T>G ENSP00000460849.2:p.Tyr2245Asp
ENST00000703537.1:c.2661T>G
ENST00000703538.1:c.*6636T>G ENSP00000515361.1:n.*6636T>G
ENST00000703539.1:n.3227T>G
ENST00000703540.1:c.6766T>G ENSP00000515362.1:p.Tyr2256Asp
ENST00000703541.1:c.6778T>G ENSP00000515363.1:p.Tyr2260Asp
ENST00000304992.11:c.6913T>G MANE Select ENSP00000304350.6:p.Tyr2305Asp
ENST00000304992.10:c.6913T>G ENSP00000304350.6:p.Tyr2305Asp
ENST00000571958.1:c.163-51T>G
ENST00000572621.5:c.6913T>G ENSP00000460348.1:p.Tyr2305Asp
ENST00000572723.1:n.902T>G
NM_006445.3:c.6913T>G NP_006436.3:p.Tyr2305Asp
XM_024450537.1:c.6913T>G XP_024306305.1:p.Tyr2305Asp
NM_006445.4:c.6913T>G MANE Select NP_006436.3:p.Tyr2305Asp