Canonical Allele Identifier: CA2739277312

Gene: UBE3B

Linked Data

• ClinVar Variation Id: 2874810
• ClinVar RCV Id: RCV003714726

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109521432del , CM000674.2:g.109521432del	GRCh38
NC_000012.11:g.109959237del , CM000674.1:g.109959237del	GRCh37
NC_000012.10:g.108443620del	NCBI36
NG_033898.1:g.48810del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342494.8:c.2254-9del MANE Select	ENSP00000340596.3:n.2254-9del
ENST00000342494.7:c.2254-9del	ENSP00000340596.3:n.2254-9del
ENST00000434735.6:c.2254-9del	ENSP00000391529.2:n.2254-9del
ENST00000449510.6:c.*224-9del	ENSP00000395802.2:n.*224-9del
ENST00000538070.1:n.1770-9del
ENST00000539584.5:n.1778-9del
ENST00000539599.5:c.2254-9del	ENSP00000443131.1:n.2254-9del
NM_130466.3:c.2254-9del	NP_569733.2:n.2254-9del
NM_183415.2:c.2254-9del	NP_904324.1:n.2254-9del
XM_005253987.1:c.2254-9del	XP_005254044.1:n.2254-9del
XM_006719681.2:c.2254-9del	XP_006719744.1:n.2254-9del
XM_006719682.1:c.2254-9del	XP_006719745.1:n.2254-9del
XM_011538959.1:c.2254-9del	XP_011537261.1:n.2254-9del
XM_011538960.1:c.2254-9del	XP_011537262.1:n.2254-9del
XM_011538961.1:c.2254-9del	XP_011537263.1:n.2254-9del
XM_011538962.1:c.2254-9del	XP_011537264.1:n.2254-9del
XR_429118.2:n.3081-9del
XM_005253987.2:c.2254-9del	XP_005254044.1:n.2254-9del
XM_006719681.3:c.2254-9del	XP_006719744.1:n.2254-9del
XM_006719682.2:c.2254-9del	XP_006719745.1:n.2254-9del
XM_011538959.2:c.2254-9del	XP_011537261.1:n.2254-9del
XM_017020195.1:c.1675-9del	XP_016875684.1:n.1675-9del
XM_024449269.1:c.1675-9del	XP_024305037.1:n.1675-9del
XR_429118.3:n.3081-9del
XR_429119.4:n.3270-9del
NM_130466.4:c.2254-9del MANE Select	NP_569733.2:n.2254-9del
NM_183415.3:c.2254-9del	NP_904324.1:n.2254-9del