Canonical Allele Identifier: CA407789831

Gene: PRPF31

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.54118418C>G , CM000681.2:g.54118418C>G	GRCh38
NC_000019.8:g.59313610C>G	NCBI36
NG_009759.1:g.8009C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_015629.4:c.140C>G MANE Select	NP_056444.3:p.Ser47Ter
ENST00000321030.9:c.140C>G MANE Select	ENSP00000324122.4:p.Ser47Ter
NM_015629.3:c.140C>G	NP_056444.3:p.Ser47Ter
ENST00000321030.8:c.140C>G	ENSP00000324122.4:p.Ser47Ter
ENST00000391755.1:c.140C>G	ENSP00000375635.1:p.Ser47Ter
ENST00000419967.5:c.140C>G	ENSP00000405166.2:p.Ser47Ter
ENST00000445124.5:c.140C>G	ENSP00000408980.1:p.Ser47Ter
ENST00000445811.5:c.140C>G	ENSP00000395894.1:p.Ser47Ter
ENST00000447810.5:c.140C>G	ENSP00000395089.1:p.Ser47Ter
ENST00000466404.5:n.10C>G
ENST00000467851.1:n.13C>G
XM_006723137.2:c.140C>G	XP_006723200.1:p.Ser47Ter
XM_006723137.4:c.140C>G	XP_006723200.1:p.Ser47Ter
XR_002958293.1:n.270C>G
XR_935789.1:n.189C>G
XR_935789.3:n.201C>G