Canonical Allele Identifier: CA309324681
Community Standard Title: NM_015629.4(PRPF31):c.429C>T (p.Gly143=)
Gene: PRPF31 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.54123462C>T , CM000681.2:g.54123462C>T GRCh38
NC_000019.8:g.59318653C>T NCBI36
NG_009759.1:g.13052C>T

Transcript Alleles

HGVS Amino-acid Change
NM_015629.4:c.429C>T MANE Select NP_056444.3:p.Gly143=
ENST00000321030.9:c.429C>T MANE Select ENSP00000324122.4:p.Gly143=
NM_015629.3:c.429C>T NP_056444.3:p.Gly143=
ENST00000321030.8:c.429C>T ENSP00000324122.4:p.Gly143=
ENST00000391755.1:c.429C>T ENSP00000375635.1:p.Gly143=
ENST00000419967.5:c.429C>T ENSP00000405166.2:p.Gly143=
ENST00000445124.5:c.429C>T ENSP00000408980.1:p.Gly143=
ENST00000445811.5:c.429C>T ENSP00000395894.1:p.Gly143=
ENST00000447810.5:c.429C>T ENSP00000395089.1:p.Gly143=
ENST00000466404.5:n.299C>T
ENST00000498612.1:n.212C>T
XM_006723137.2:c.429C>T XP_006723200.1:p.Gly143=
XM_006723137.4:c.429C>T XP_006723200.1:p.Gly143=
XR_002958293.1:n.559C>T
XR_935789.1:n.478C>T
XR_935789.3:n.490C>T