Canonical Allele Identifier: CA2242977095
Gene: PRPF8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1650765C= , CM000679.2:g.1650765C= GRCh38
NC_000017.10:g.1554059C= , CM000679.1:g.1554059C= GRCh37
NC_000017.9:g.1500809C= NCBI36
NG_009118.1:g.39118G=
NG_033061.1:g.4334G=

Transcript Alleles

HGVS Amino-acid change
ENST00000573725.2:c.*37G= ENSP00000460849.2:n.*37G=
ENST00000703537.1:c.2793G=
ENST00000703538.1:c.*6768G= ENSP00000515361.1:n.*6768G=
ENST00000703539.1:n.3359G=
ENST00000703540.1:c.*37G= ENSP00000515362.1:n.*37G=
ENST00000304992.11:c.*37G= MANE Select ENSP00000304350.6:n.*37G=
ENST00000304992.10:c.*37G= ENSP00000304350.6:n.*37G=
ENST00000571958.1:c.244G=
ENST00000572621.5:c.*37G= ENSP00000460348.1:n.*37G=
NM_006445.3:c.*37G= NP_006436.3:n.*37G=
XM_024450537.1:c.*37G= XP_024306305.1:n.*37G=
NM_006445.4:c.*37G= MANE Select NP_006436.3:n.*37G=