Canonical Allele Identifier: CA325622
Gene: UBE3A HGNC NCBI
SNHG14 HGNC NCBI

Linked Data

ClinVar Variation Id: 7967
ClinVar RCV Id: RCV000008431
dbSNP Id: rs111033595

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.25340219C>T , CM000677.2:g.25340219C>T GRCh38
NC_000015.9:g.25585366C>T , CM000677.1:g.25585366C>T GRCh37
NC_000015.8:g.23136459C>T NCBI36
NG_009268.1:g.103763G>A , LRG_15:g.103763G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000438097.6:c.2304G>A (UBE3A) ENSP00000411258.1:p.Trp768Ter
ENST00000635914.1:c.2304G>A (UBE3A) ENSP00000490563.1:p.Trp768Ter
ENST00000636667.1:c.-100G>A (UBE3A) ENSP00000489625.1:n.-100G>A
ENST00000637886.1:c.2364G>A (UBE3A) ENSP00000490258.1:p.Trp788Ter
ENST00000638011.1:c.2304G>A (UBE3A) ENSP00000490111.1:p.Trp768Ter
ENST00000638155.1:c.2304G>A (UBE3A) ENSP00000490557.1:p.Trp768Ter
ENST00000648336.2:c.2364G>A (UBE3A) MANE Select ENSP00000497572.2:p.Trp788Ter
ENST00000649550.1:c.2304G>A (UBE3A) ENSP00000497549.1:p.Trp768Ter
ENST00000650110.1:c.2373G>A (UBE3A) ENSP00000497594.1:p.Trp791Ter
ENST00000675177.1:c.2187G>A (UBE3A) ENSP00000502703.1:p.Trp729Ter
ENST00000675593.1:n.5060G>A (UBE3A)
ENST00000232165.7:c.2304G>A (UBE3A) ENSP00000232165.5:p.Trp768Ter
ENST00000397954.6:c.2373G>A (UBE3A) ENSP00000381045.2:p.Trp791Ter
ENST00000428984.6:c.2304G>A (UBE3A) ENSP00000401265.2:p.Trp768Ter
ENST00000438097.5:c.2304G>A (UBE3A) ENSP00000411258.1:p.Trp768Ter
ENST00000566215.5:c.2304G>A (UBE3A) ENSP00000457771.1:p.Trp768Ter
ENST00000604860.3:c.315G>A (UBE3A) ENSP00000473822.2:p.Trp105Ter
ENST00000614096.4:c.2364G>A (UBE3A) ENSP00000481796.1:p.Trp788Ter
ENST00000626176.2:c.175G>A (UBE3A)
ENST00000630424.2:c.2304G>A (UBE3A) ENSP00000486349.1:p.Trp768Ter
NM_000462.3:c.2373G>A (UBE3A) NP_000453.2:p.Trp791Ter
NM_130838.1:c.2304G>A , LRG_15t1:c.2304G>A (UBE3A) NP_570853.1:p.Trp768Ter
NM_130839.2:c.2364G>A (UBE3A) NP_570854.1:p.Trp788Ter
XM_005268267.3:c.2304G>A (UBE3A) XP_005268324.1:p.Trp768Ter
XM_005268268.3:c.2304G>A (UBE3A) XP_005268325.1:p.Trp768Ter
XM_005268269.3:c.2304G>A (UBE3A) XP_005268326.1:p.Trp768Ter
XM_005268270.3:c.2304G>A (UBE3A) XP_005268327.1:p.Trp768Ter
XM_005268271.3:c.2304G>A (UBE3A) XP_005268328.1:p.Trp768Ter
XM_006720673.2:c.2364G>A (UBE3A) XP_006720736.1:p.Trp788Ter
XM_006720674.2:c.2364G>A (UBE3A) XP_006720737.1:p.Trp788Ter
XM_006720675.2:c.2304G>A (UBE3A) XP_006720738.1:p.Trp768Ter
XM_006720676.2:c.2304G>A (UBE3A) XP_006720739.1:p.Trp768Ter
XM_011521994.1:c.2373G>A (UBE3A) XP_011520296.1:p.Trp791Ter
XM_011521995.1:c.2373G>A (UBE3A) XP_011520297.1:p.Trp791Ter
XM_011521996.1:c.2304G>A (UBE3A) XP_011520298.1:p.Trp768Ter
NM_000462.5:c.2373G>A (UBE3A) NP_000453.2:p.Trp791Ter
NM_001354505.1:c.2364G>A (UBE3A) NP_001341434.1:p.Trp788Ter
NM_001354506.1:c.2304G>A (UBE3A) NP_001341435.1:p.Trp768Ter
NM_001354507.1:c.2304G>A (UBE3A) NP_001341436.1:p.Trp768Ter
NM_001354508.1:c.2304G>A (UBE3A) NP_001341437.1:p.Trp768Ter
NM_001354509.1:c.2304G>A (UBE3A) NP_001341438.1:p.Trp768Ter
NM_001354511.1:c.2304G>A (UBE3A) NP_001341440.1:p.Trp768Ter
NM_001354512.1:c.2304G>A (UBE3A) NP_001341441.1:p.Trp768Ter
NM_001354513.1:c.2304G>A (UBE3A) NP_001341442.1:p.Trp768Ter
NM_001354523.1:c.2304G>A (UBE3A) NP_001341452.1:p.Trp768Ter
NM_001354526.1:c.2304G>A (UBE3A) NP_001341455.1:p.Trp768Ter
NM_001354538.1:c.2364G>A (UBE3A) NP_001341467.1:p.Trp788Ter
NM_001354539.1:c.2304G>A (UBE3A) NP_001341468.1:p.Trp768Ter
NM_001354540.1:c.2304G>A (UBE3A) NP_001341469.1:p.Trp768Ter
NM_001354541.1:c.2304G>A (UBE3A) NP_001341470.1:p.Trp768Ter
NM_001354542.1:c.2304G>A (UBE3A) NP_001341471.1:p.Trp768Ter
NM_001354543.1:c.2304G>A (UBE3A) NP_001341472.1:p.Trp768Ter
NM_001354544.1:c.2304G>A (UBE3A) NP_001341473.1:p.Trp768Ter
NM_001354545.1:c.2208G>A (UBE3A) NP_001341474.1:p.Trp736Ter
NM_001354546.1:c.2187G>A (UBE3A) NP_001341475.1:p.Trp729Ter
NM_001354547.1:c.2148G>A (UBE3A) NP_001341476.1:p.Trp716Ter
NM_001354548.1:c.2148G>A (UBE3A) NP_001341477.1:p.Trp716Ter
NM_001354549.1:c.2139G>A (UBE3A) NP_001341478.1:p.Trp713Ter
NM_001354550.1:c.1113G>A (UBE3A) NP_001341479.1:p.Trp371Ter
NM_001354551.1:c.1053G>A (UBE3A) NP_001341480.1:p.Trp351Ter
NM_130838.3:c.2304G>A (UBE3A) NP_570853.1:p.Trp768Ter
NM_130839.4:c.2364G>A (UBE3A) NP_570854.1:p.Trp788Ter
NR_146177.1:n.18393-51377C>T (SNHG14)
NR_148916.1:n.2908G>A (UBE3A)
XM_011521995.3:c.2373G>A (UBE3A) XP_011520297.1:p.Trp791Ter
XM_017022547.2:c.2364G>A (UBE3A) XP_016878036.1:p.Trp788Ter
XM_017022548.2:c.2364G>A (UBE3A) XP_016878037.1:p.Trp788Ter
XM_017022550.2:c.2364G>A (UBE3A) XP_016878039.1:p.Trp788Ter
XM_017022556.2:c.2217G>A (UBE3A) XP_016878045.1:p.Trp739Ter
XM_024450043.1:c.2373G>A (UBE3A) XP_024305811.1:p.Trp791Ter
XM_024450044.1:c.2304G>A (UBE3A) XP_024305812.1:p.Trp768Ter
NM_001354506.2:c.2304G>A (UBE3A) NP_001341435.1:p.Trp768Ter
NM_001354507.2:c.2304G>A (UBE3A) NP_001341436.1:p.Trp768Ter
NM_001354508.2:c.2304G>A (UBE3A) NP_001341437.1:p.Trp768Ter
NM_001354509.2:c.2304G>A (UBE3A) NP_001341438.1:p.Trp768Ter
NM_001354511.2:c.2304G>A (UBE3A) NP_001341440.1:p.Trp768Ter
NM_001354512.2:c.2304G>A (UBE3A) NP_001341441.1:p.Trp768Ter
NM_001354513.2:c.2304G>A (UBE3A) NP_001341442.1:p.Trp768Ter
NM_001354523.2:c.2304G>A (UBE3A) NP_001341452.1:p.Trp768Ter
NM_001354538.2:c.2364G>A (UBE3A) NP_001341467.1:p.Trp788Ter
NM_001354539.2:c.2304G>A (UBE3A) NP_001341468.1:p.Trp768Ter
NM_001354540.2:c.2304G>A (UBE3A) NP_001341469.1:p.Trp768Ter
NM_001354541.2:c.2304G>A (UBE3A) NP_001341470.1:p.Trp768Ter
NM_001354542.2:c.2304G>A (UBE3A) NP_001341471.1:p.Trp768Ter
NM_001354543.2:c.2304G>A (UBE3A) NP_001341472.1:p.Trp768Ter
NM_001354544.2:c.2304G>A (UBE3A) NP_001341473.1:p.Trp768Ter
NM_001354545.2:c.2208G>A (UBE3A) NP_001341474.1:p.Trp736Ter
NM_001354546.2:c.2187G>A (UBE3A) NP_001341475.1:p.Trp729Ter
NM_001354547.2:c.2148G>A (UBE3A) NP_001341476.1:p.Trp716Ter
NM_001354548.2:c.2148G>A (UBE3A) NP_001341477.1:p.Trp716Ter
NM_001354549.2:c.2139G>A (UBE3A) NP_001341478.1:p.Trp713Ter
NM_001354550.2:c.1113G>A (UBE3A) NP_001341479.1:p.Trp371Ter
NM_001354551.2:c.1053G>A (UBE3A) NP_001341480.1:p.Trp351Ter
NM_001374461.1:c.2304G>A (UBE3A) NP_001361390.1:p.Trp768Ter
NM_130838.4:c.2304G>A (UBE3A) NP_570853.1:p.Trp768Ter
NM_130839.5:c.2364G>A (UBE3A) MANE Select NP_570854.1:p.Trp788Ter
NR_148916.2:n.2876G>A (UBE3A)