Canonical Allele Identifier: CA715751555

Gene: UBE2Q2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.75866642G>T , CM000677.2:g.75866642G>T	GRCh38
NC_000015.9:g.76158983G>T , CM000677.1:g.76158983G>T	GRCh37
NC_000015.8:g.73946038G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267938.9:c.388-2309G>T MANE Select	ENSP00000267938.4:n.388-2309G>T
ENST00000267938.8:c.388-2309G>T	ENSP00000267938.4:n.388-2309G>T
ENST00000426727.6:c.44-2309G>T
ENST00000561723.5:c.282+12155G>T	ENSP00000458006.1:n.282+12155G>T
ENST00000561851.5:c.340-2309G>T	ENSP00000456229.1:n.340-2309G>T
ENST00000569423.5:c.283-2309G>T	ENSP00000456324.1:n.283-2309G>T
NM_001145335.1:c.340-2309G>T	NP_001138807.1:n.340-2309G>T
NM_001284382.1:c.283-2309G>T	NP_001271311.1:n.283-2309G>T
NM_173469.3:c.388-2309G>T	NP_775740.1:n.388-2309G>T
XM_005254787.1:c.388-2309G>T	XP_005254844.1:n.388-2309G>T
XM_005254788.1:c.388-2309G>T	XP_005254845.1:n.388-2309G>T
XM_006720770.1:c.388-2309G>T	XP_006720833.1:n.388-2309G>T
XM_011522227.1:c.388-2309G>T	XP_011520529.1:n.388-2309G>T
XM_011522228.1:c.388-2309G>T	XP_011520530.1:n.388-2309G>T
XR_931947.1:n.541-2309G>T
XM_005254787.2:c.388-2309G>T	XP_005254844.1:n.388-2309G>T
XM_005254788.2:c.388-2309G>T	XP_005254845.1:n.388-2309G>T
XM_006720770.2:c.388-2309G>T	XP_006720833.1:n.388-2309G>T
XM_011522228.2:c.388-2309G>T	XP_011520530.1:n.388-2309G>T
XM_017022726.1:c.340-2309G>T	XP_016878215.1:n.340-2309G>T
XM_017022727.2:c.283-2309G>T	XP_016878216.1:n.283-2309G>T
XM_017022728.2:c.283-2309G>T	XP_016878217.1:n.283-2309G>T
XM_024450107.1:c.388-2309G>T	XP_024305875.1:n.388-2309G>T
XM_024450108.1:c.388-2309G>T	XP_024305876.1:n.388-2309G>T
XR_001751420.2:n.712-2309G>T
XR_001751421.2:n.712-2309G>T
XR_002957691.1:n.712-2309G>T
XR_002957692.1:n.712-2309G>T
NM_001284382.2:c.283-2309G>T	NP_001271311.1:n.283-2309G>T
NM_173469.4:c.388-2309G>T MANE Select	NP_775740.1:n.388-2309G>T