Canonical Allele Identifier: CA309328013
Gene: PRPF31 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.54126607C>T , CM000681.2:g.54126607C>T GRCh38
NC_000019.8:g.59321794C>T NCBI36
NG_009759.1:g.16193C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000321030.9:c.935C>T MANE Select ENSP00000324122.4:p.Thr312Ile
ENST00000321030.8:c.935C>T ENSP00000324122.4:p.Thr312Ile
ENST00000391755.1:c.935C>T ENSP00000375635.1:p.Thr312Ile
ENST00000419967.5:c.935C>T ENSP00000405166.2:p.Thr312Ile
ENST00000466404.5:n.805C>T
ENST00000498612.1:n.746C>T
NM_015629.3:c.935C>T NP_056444.3:p.Thr312Ile
XM_006723137.2:c.935C>T XP_006723200.1:p.Thr312Ile
XR_935789.1:n.1012C>T
XM_006723137.4:c.935C>T XP_006723200.1:p.Thr312Ile
XR_002958293.1:n.1093C>T
XR_935789.3:n.1024C>T
NM_015629.4:c.935C>T MANE Select NP_056444.3:p.Thr312Ile