Canonical Allele Identifier: CA309324676

Gene: PRPF31

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.54123445C>T , CM000681.2:g.54123445C>T	GRCh38
NC_000019.8:g.59318636C>T	NCBI36
NG_009759.1:g.13035C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_015629.4:c.421-9C>T MANE Select	NP_056444.3:n.421-9C>T
ENST00000321030.9:c.421-9C>T MANE Select	ENSP00000324122.4:n.421-9C>T
NM_015629.3:c.421-9C>T	NP_056444.3:n.421-9C>T
ENST00000321030.8:c.421-9C>T	ENSP00000324122.4:n.421-9C>T
ENST00000391755.1:c.421-9C>T	ENSP00000375635.1:n.421-9C>T
ENST00000419967.5:c.421-9C>T	ENSP00000405166.2:n.421-9C>T
ENST00000445124.5:c.421-9C>T	ENSP00000408980.1:n.421-9C>T
ENST00000445811.5:c.421-9C>T	ENSP00000395894.1:n.421-9C>T
ENST00000447810.5:c.421-9C>T	ENSP00000395089.1:n.421-9C>T
ENST00000466404.5:n.291-9C>T
ENST00000498612.1:n.204-9C>T
XM_006723137.2:c.421-9C>T	XP_006723200.1:n.421-9C>T
XM_006723137.4:c.421-9C>T	XP_006723200.1:n.421-9C>T
XR_002958293.1:n.551-9C>T
XR_935789.1:n.470-9C>T
XR_935789.3:n.482-9C>T