Canonical Allele Identifier: CA407754036

Gene: PRPF31

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.54128372G>T , CM000681.2:g.54128372G>T	GRCh38
NC_000019.8:g.59323559G>T	NCBI36
NG_009759.1:g.17958G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_015629.4:c.1141G>T MANE Select	NP_056444.3:p.Gly381Ter
ENST00000321030.9:c.1141G>T MANE Select	ENSP00000324122.4:p.Gly381Ter
NM_015629.3:c.1141G>T	NP_056444.3:p.Gly381Ter
ENST00000321030.8:c.1141G>T	ENSP00000324122.4:p.Gly381Ter
ENST00000391755.1:c.1123G>T	ENSP00000375635.1:p.Gly375Ter
ENST00000419967.5:c.1141G>T	ENSP00000405166.2:p.Gly381Ter
ENST00000466404.5:n.1115G>T
XM_006723137.2:c.1141G>T	XP_006723200.1:p.Gly381Ter
XM_006723137.4:c.1141G>T	XP_006723200.1:p.Gly381Ter
XR_002958293.1:n.1299G>T
XR_935789.1:n.1218G>T
XR_935789.3:n.1230G>T