Canonical Allele Identifier: CA2809501265
Gene: JUP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41758923_41758924insAAT , CM000679.2:g.41758923_41758924insAAT GRCh38
NC_000017.10:g.39915175_39915176insAAT , CM000679.1:g.39915175_39915176insAAT GRCh37
NC_000017.9:g.37168701_37168702insAAT NCBI36
NG_009090.2:g.32789_32790insATT , LRG_401:g.32789_32790insATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000393931.8:c.1498-54_1498-53insATT MANE Select ENSP00000377508.3:n.1498-54_1498-53insATT
ENST00000310706.9:c.1498-54_1498-53insATT ENSP00000311113.5:n.1498-54_1498-53insATT
ENST00000393930.5:c.1498-54_1498-53insATT ENSP00000377507.1:n.1498-54_1498-53insATT
ENST00000393931.7:c.1498-54_1498-53insATT ENSP00000377508.3:n.1498-54_1498-53insATT
ENST00000585793.1:n.96-54_96-53insATT
NM_002230.2:c.1498-54_1498-53insATT , LRG_401t2:c.1498-54_1498-53insATT NP_002221.1:n.1498-54_1498-53insATT
NM_021991.2:c.1498-54_1498-53insATT , LRG_401t1:c.1498-54_1498-53insATT NP_068831.1:n.1498-54_1498-53insATT
XM_006721873.1:c.1498-54_1498-53insATT XP_006721936.1:n.1498-54_1498-53insATT
XM_006721874.1:c.1498-54_1498-53insATT XP_006721937.1:n.1498-54_1498-53insATT
XM_006721875.1:c.1498-54_1498-53insATT XP_006721938.1:n.1498-54_1498-53insATT
XM_006721878.1:c.1498-54_1498-53insATT XP_006721941.1:n.1498-54_1498-53insATT
XM_011524753.1:c.1498-54_1498-53insATT XP_011523055.1:n.1498-54_1498-53insATT
XM_011524754.1:c.1498-54_1498-53insATT XP_011523056.1:n.1498-54_1498-53insATT
XM_011524755.1:c.1498-54_1498-53insATT XP_011523057.1:n.1498-54_1498-53insATT
XM_011524756.1:c.1498-54_1498-53insATT XP_011523058.1:n.1498-54_1498-53insATT
XM_011524757.1:c.1498-54_1498-53insATT XP_011523059.1:n.1498-54_1498-53insATT
XM_011524758.1:c.1498-54_1498-53insATT XP_011523060.1:n.1498-54_1498-53insATT
NM_001352773.1:c.1498-54_1498-53insATT NP_001339702.1:n.1498-54_1498-53insATT
NM_001352774.1:c.1498-54_1498-53insATT NP_001339703.1:n.1498-54_1498-53insATT
NM_001352775.1:c.1498-54_1498-53insATT NP_001339704.1:n.1498-54_1498-53insATT
NM_001352776.1:c.1498-54_1498-53insATT NP_001339705.1:n.1498-54_1498-53insATT
NM_001352777.1:c.1498-54_1498-53insATT NP_001339706.1:n.1498-54_1498-53insATT
NM_002230.3:c.1498-54_1498-53insATT NP_002221.1:n.1498-54_1498-53insATT
NM_021991.3:c.1498-54_1498-53insATT NP_068831.1:n.1498-54_1498-53insATT
XM_006721874.3:c.1498-54_1498-53insATT XP_006721937.1:n.1498-54_1498-53insATT
XM_011524753.2:c.1498-54_1498-53insATT XP_011523055.1:n.1498-54_1498-53insATT
XM_017024588.2:c.1549-54_1549-53insATT XP_016880077.1:n.1549-54_1549-53insATT
XM_017024590.1:c.1498-54_1498-53insATT XP_016880079.1:n.1498-54_1498-53insATT
NM_002230.4:c.1498-54_1498-53insATT MANE Select NP_002221.1:n.1498-54_1498-53insATT
NM_001352773.2:c.1498-54_1498-53insATT NP_001339702.1:n.1498-54_1498-53insATT
NM_001352774.2:c.1498-54_1498-53insATT NP_001339703.1:n.1498-54_1498-53insATT
NM_001352775.2:c.1498-54_1498-53insATT NP_001339704.1:n.1498-54_1498-53insATT
NM_001352776.2:c.1498-54_1498-53insATT NP_001339705.1:n.1498-54_1498-53insATT
NM_001352777.2:c.1498-54_1498-53insATT NP_001339706.1:n.1498-54_1498-53insATT
NM_021991.4:c.1498-54_1498-53insATT NP_068831.1:n.1498-54_1498-53insATT