Canonical Allele Identifier: CA1959806

Gene: UBR3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169872330A>G , CM000664.2:g.169872330A>G	GRCh38
NC_000002.11:g.170728840A>G , CM000664.1:g.170728840A>G	GRCh37
NC_000002.10:g.170437086A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_172070.4:c.640A>G MANE Select	NP_742067.3:p.Ile214Val
ENST00000272793.11:c.640A>G MANE Select	ENSP00000272793.5:p.Ile214Val
NM_172070.3:c.640A>G	NP_742067.3:p.Ile214Val
ENST00000272793.9:c.640A>G	ENSP00000272793.5:p.Ile214Val
ENST00000418381.5:c.640A>G	ENSP00000396068.1:p.Ile214Val
XM_005246299.3:c.640A>G	XP_005246356.1:p.Ile214Val
XM_005246299.4:c.640A>G	XP_005246356.1:p.Ile214Val
XM_005246300.3:c.640A>G	XP_005246357.1:p.Ile214Val
XM_005246300.4:c.640A>G	XP_005246357.1:p.Ile214Val
XM_006712268.2:c.640A>G	XP_006712331.1:p.Ile214Val
XM_006712268.4:c.640A>G	XP_006712331.1:p.Ile214Val
XM_006712269.2:c.640A>G	XP_006712332.1:p.Ile214Val
XM_006712269.3:c.640A>G	XP_006712332.1:p.Ile214Val
XM_006712270.2:c.640A>G	XP_006712333.2:p.Ile214Val
XM_006712270.3:c.640A>G	XP_006712333.2:p.Ile214Val
XM_006712271.2:c.640A>G	XP_006712334.1:p.Ile214Val
XM_006712271.4:c.640A>G	XP_006712334.1:p.Ile214Val
XM_011510604.1:c.640A>G	XP_011508906.1:p.Ile214Val
XM_011510604.2:c.640A>G	XP_011508906.1:p.Ile214Val
XM_017003356.2:c.640A>G	XP_016858845.1:p.Ile214Val
XM_017003357.1:c.640A>G	XP_016858846.1:p.Ile214Val
XM_017003358.1:c.640A>G	XP_016858847.1:p.Ile214Val
XM_017003359.1:c.640A>G	XP_016858848.1:p.Ile214Val
XR_922841.1:n.673A>G
XR_922841.2:n.640A>G
XR_922842.1:n.678A>G