Canonical Allele Identifier: CA2242977107
Gene: PRPF8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1650770T= , CM000679.2:g.1650770T= GRCh38
NC_000017.10:g.1554064T= , CM000679.1:g.1554064T= GRCh37
NC_000017.9:g.1500814T= NCBI36
NG_009118.1:g.39113A=
NG_033061.1:g.4329A=

Transcript Alleles

HGVS Amino-acid change
ENST00000573725.2:c.*32A= ENSP00000460849.2:n.*32A=
ENST00000703537.1:c.2788A=
ENST00000703538.1:c.*6763A= ENSP00000515361.1:n.*6763A=
ENST00000703539.1:n.3354A=
ENST00000703540.1:c.*32A= ENSP00000515362.1:n.*32A=
ENST00000304992.11:c.*32A= MANE Select ENSP00000304350.6:n.*32A=
ENST00000304992.10:c.*32A= ENSP00000304350.6:n.*32A=
ENST00000571958.1:c.239A=
ENST00000572621.5:c.*32A= ENSP00000460348.1:n.*32A=
NM_006445.3:c.*32A= NP_006436.3:n.*32A=
XM_024450537.1:c.*32A= XP_024306305.1:n.*32A=
NM_006445.4:c.*32A= MANE Select NP_006436.3:n.*32A=