Canonical Allele Identifier: CA4832229

Gene: UBR5

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102295206G>A , CM000670.2:g.102295206G>A	GRCh38
NC_000008.10:g.103307434G>A , CM000670.1:g.103307434G>A	GRCh37
NC_000008.9:g.103376610G>A	NCBI36
NG_047152.1:g.122484C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000520539.6:c.4056C>T MANE Select	ENSP00000429084.1:p.Asp1352=
ENST00000220959.8:c.4056C>T	ENSP00000220959.4:p.Asp1352=
ENST00000520539.5:c.4056C>T	ENSP00000429084.1:p.Asp1352=
ENST00000521922.5:c.4038C>T	ENSP00000427819.1:p.Asp1346=
NM_001282873.1:c.4056C>T	NP_001269802.1:p.Asp1352=
NM_015902.5:c.4056C>T	NP_056986.2:p.Asp1352=
XM_005250962.3:c.1086C>T	XP_005251019.1:p.Asp362=
XM_011517104.1:c.3312C>T	XP_011515406.1:p.Asp1104=
XM_011517105.1:c.3312C>T	XP_011515407.1:p.Asp1104=
XM_011517106.1:c.3294C>T	XP_011515408.1:p.Asp1098=
XM_005250962.5:c.1086C>T	XP_005251019.1:p.Asp362=
XM_011517104.3:c.4011C>T	XP_011515406.2:p.Asp1337=
XM_011517105.3:c.4011C>T	XP_011515407.2:p.Asp1337=
XM_011517106.3:c.3993C>T	XP_011515408.2:p.Asp1331=
XM_017013533.2:c.4011C>T	XP_016869022.1:p.Asp1337=
XM_017013534.2:c.4011C>T	XP_016869023.1:p.Asp1337=
XM_024447178.1:c.3312C>T	XP_024302946.1:p.Asp1104=
XM_024447179.1:c.3294C>T	XP_024302947.1:p.Asp1098=
XR_001745539.2:n.4030C>T
XR_001745540.2:n.4030C>T
XR_001745541.2:n.4030C>T
NM_015902.6:c.4056C>T MANE Select	NP_056986.2:p.Asp1352=
NM_001282873.2:c.4056C>T	NP_001269802.1:p.Asp1352=