Canonical Allele Identifier: CA407751772

Gene: PRPF31

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.54126527G>A , CM000681.2:g.54126527G>A	GRCh38
NC_000019.8:g.59321714G>A	NCBI36
NG_009759.1:g.16113G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015629.4:c.856-1G>A MANE Select	NP_056444.3:n.856-1G>A
ENST00000321030.9:c.856-1G>A MANE Select	ENSP00000324122.4:n.856-1G>A
NM_015629.3:c.856-1G>A	NP_056444.3:n.856-1G>A
ENST00000321030.8:c.856-1G>A	ENSP00000324122.4:n.856-1G>A
ENST00000391755.1:c.856-1G>A	ENSP00000375635.1:n.856-1G>A
ENST00000419967.5:c.856-1G>A	ENSP00000405166.2:n.856-1G>A
ENST00000466404.5:n.726-1G>A
ENST00000498612.1:n.666G>A
XM_006723137.2:c.856-1G>A	XP_006723200.1:n.856-1G>A
XM_006723137.4:c.856-1G>A	XP_006723200.1:n.856-1G>A
XR_002958293.1:n.1013G>A
XR_935789.1:n.932G>A
XR_935789.3:n.944G>A