Canonical Allele Identifier: CA2797410929
Gene: UBE3B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.109521355_109521356insAATTA , CM000674.2:g.109521355_109521356insAATTA GRCh38
NC_000012.11:g.109959160_109959161insAATTA , CM000674.1:g.109959160_109959161insAATTA GRCh37
NC_000012.10:g.108443543_108443544insAATTA NCBI36
NG_033898.1:g.48733_48734insAATTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000342494.8:c.2253+31_2253+32insAATTA MANE Select ENSP00000340596.3:n.2253+31_2253+32insAATTA
ENST00000342494.7:c.2253+31_2253+32insAATTA ENSP00000340596.3:n.2253+31_2253+32insAATTA
ENST00000434735.6:c.2253+31_2253+32insAATTA ENSP00000391529.2:n.2253+31_2253+32insAATTA
ENST00000449510.6:c.*223+31_*223+32insAATTA ENSP00000395802.2:n.*223+31_*223+32insAATTA
ENST00000538070.1:n.1769+31_1769+32insAATTA
ENST00000539584.5:n.1777+31_1777+32insAATTA
ENST00000539599.5:c.2253+31_2253+32insAATTA ENSP00000443131.1:n.2253+31_2253+32insAATTA
NM_130466.3:c.2253+31_2253+32insAATTA NP_569733.2:n.2253+31_2253+32insAATTA
NM_183415.2:c.2253+31_2253+32insAATTA NP_904324.1:n.2253+31_2253+32insAATTA
XM_005253987.1:c.2253+31_2253+32insAATTA XP_005254044.1:n.2253+31_2253+32insAATTA
XM_006719681.2:c.2253+31_2253+32insAATTA XP_006719744.1:n.2253+31_2253+32insAATTA
XM_006719682.1:c.2253+31_2253+32insAATTA XP_006719745.1:n.2253+31_2253+32insAATTA
XM_011538959.1:c.2253+31_2253+32insAATTA XP_011537261.1:n.2253+31_2253+32insAATTA
XM_011538960.1:c.2253+31_2253+32insAATTA XP_011537262.1:n.2253+31_2253+32insAATTA
XM_011538961.1:c.2253+31_2253+32insAATTA XP_011537263.1:n.2253+31_2253+32insAATTA
XM_011538962.1:c.2253+31_2253+32insAATTA XP_011537264.1:n.2253+31_2253+32insAATTA
XR_429118.2:n.3080+31_3080+32insAATTA
XM_005253987.2:c.2253+31_2253+32insAATTA XP_005254044.1:n.2253+31_2253+32insAATTA
XM_006719681.3:c.2253+31_2253+32insAATTA XP_006719744.1:n.2253+31_2253+32insAATTA
XM_006719682.2:c.2253+31_2253+32insAATTA XP_006719745.1:n.2253+31_2253+32insAATTA
XM_011538959.2:c.2253+31_2253+32insAATTA XP_011537261.1:n.2253+31_2253+32insAATTA
XM_017020195.1:c.1674+31_1674+32insAATTA XP_016875684.1:n.1674+31_1674+32insAATTA
XM_024449269.1:c.1674+31_1674+32insAATTA XP_024305037.1:n.1674+31_1674+32insAATTA
XR_429118.3:n.3080+31_3080+32insAATTA
XR_429119.4:n.3269+31_3269+32insAATTA
NM_130466.4:c.2253+31_2253+32insAATTA MANE Select NP_569733.2:n.2253+31_2253+32insAATTA
NM_183415.3:c.2253+31_2253+32insAATTA NP_904324.1:n.2253+31_2253+32insAATTA