Canonical Allele Identifier: CA2809501796
Gene: JUP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41771963_41771964insCAAACACACCCAACAC , CM000679.2:g.41771963_41771964insCAAACACACCCAACAC GRCh38
NC_000017.10:g.39928215_39928216insCAAACACACCCAACAC , CM000679.1:g.39928215_39928216insCAAACACACCCAACAC GRCh37
NC_000017.9:g.37181741_37181742insCAAACACACCCAACAC NCBI36
NG_009090.2:g.19750_19751insTGTTGGGTGTGTTTGG , LRG_401:g.19750_19751insTGTTGGGTGTGTTTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000393931.8:c.-8-101_-8-100insTGTTGGGTGTGTTTGG MANE Select ENSP00000377508.3:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
ENST00000310706.9:c.-8-101_-8-100insTGTTGGGTGTGTTTGG ENSP00000311113.5:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
ENST00000393930.5:c.-8-101_-8-100insTGTTGGGTGTGTTTGG ENSP00000377507.1:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
ENST00000393931.7:c.-8-101_-8-100insTGTTGGGTGTGTTTGG ENSP00000377508.3:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
ENST00000420370.5:c.-8-101_-8-100insTGTTGGGTGTGTTTGG ENSP00000411449.1:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
ENST00000424457.5:c.-8-101_-8-100insTGTTGGGTGTGTTTGG ENSP00000401034.1:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
ENST00000437187.5:c.-8-101_-8-100insTGTTGGGTGTGTTTGG ENSP00000394146.1:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
ENST00000437369.5:c.-8-101_-8-100insTGTTGGGTGTGTTTGG ENSP00000409948.1:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
ENST00000449889.5:c.-8-101_-8-100insTGTTGGGTGTGTTTGG ENSP00000389886.1:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
ENST00000465293.1:c.-8-101_-8-100insTGTTGGGTGTGTTTGG ENSP00000467065.1:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
ENST00000589036.1:n.124-104_124-103insTGTTGGGTGTGTTTGG
ENST00000591690.5:c.-8-101_-8-100insTGTTGGGTGTGTTTGG ENSP00000468347.1:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
NM_002230.2:c.-8-101_-8-100insTGTTGGGTGTGTTTGG , LRG_401t2:c.-8-101_-8-100insTGTTGGGTGTGTTTGG NP_002221.1:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
NM_021991.2:c.-8-101_-8-100insTGTTGGGTGTGTTTGG , LRG_401t1:c.-8-101_-8-100insTGTTGGGTGTGTTTGG NP_068831.1:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
XM_006721873.1:c.-8-101_-8-100insTGTTGGGTGTGTTTGG XP_006721936.1:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
XM_006721874.1:c.-8-101_-8-100insTGTTGGGTGTGTTTGG XP_006721937.1:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
XM_006721875.1:c.-8-101_-8-100insTGTTGGGTGTGTTTGG XP_006721938.1:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
XM_006721878.1:c.-8-101_-8-100insTGTTGGGTGTGTTTGG XP_006721941.1:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
XM_011524753.1:c.-8-101_-8-100insTGTTGGGTGTGTTTGG XP_011523055.1:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
XM_011524754.1:c.-8-101_-8-100insTGTTGGGTGTGTTTGG XP_011523056.1:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
XM_011524755.1:c.-5-104_-5-103insTGTTGGGTGTGTTTGG XP_011523057.1:n.-5-104_-5-103insTGTTGGGTGTGTTTGG
XM_011524756.1:c.-5-104_-5-103insTGTTGGGTGTGTTTGG XP_011523058.1:n.-5-104_-5-103insTGTTGGGTGTGTTTGG
XM_011524757.1:c.-5-104_-5-103insTGTTGGGTGTGTTTGG XP_011523059.1:n.-5-104_-5-103insTGTTGGGTGTGTTTGG
XM_011524758.1:c.-5-104_-5-103insTGTTGGGTGTGTTTGG XP_011523060.1:n.-5-104_-5-103insTGTTGGGTGTGTTTGG
NM_001352773.1:c.-8-101_-8-100insTGTTGGGTGTGTTTGG NP_001339702.1:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
NM_001352774.1:c.-5-104_-5-103insTGTTGGGTGTGTTTGG NP_001339703.1:n.-5-104_-5-103insTGTTGGGTGTGTTTGG
NM_001352775.1:c.-5-104_-5-103insTGTTGGGTGTGTTTGG NP_001339704.1:n.-5-104_-5-103insTGTTGGGTGTGTTTGG
NM_001352776.1:c.-8-101_-8-100insTGTTGGGTGTGTTTGG NP_001339705.1:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
NM_001352777.1:c.-8-101_-8-100insTGTTGGGTGTGTTTGG NP_001339706.1:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
NM_002230.3:c.-8-101_-8-100insTGTTGGGTGTGTTTGG NP_002221.1:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
NM_021991.3:c.-8-101_-8-100insTGTTGGGTGTGTTTGG NP_068831.1:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
XM_006721874.3:c.-8-101_-8-100insTGTTGGGTGTGTTTGG XP_006721937.1:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
XM_011524753.2:c.-8-101_-8-100insTGTTGGGTGTGTTTGG XP_011523055.1:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
XM_017024588.2:c.44-101_44-100insTGTTGGGTGTGTTTGG XP_016880077.1:n.44-101_44-100insTGTTGGGTGTGTTTGG
XM_017024590.1:c.-5-104_-5-103insTGTTGGGTGTGTTTGG XP_016880079.1:n.-5-104_-5-103insTGTTGGGTGTGTTTGG
NM_002230.4:c.-8-101_-8-100insTGTTGGGTGTGTTTGG MANE Select NP_002221.1:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
NM_001352773.2:c.-8-101_-8-100insTGTTGGGTGTGTTTGG NP_001339702.1:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
NM_001352774.2:c.-5-104_-5-103insTGTTGGGTGTGTTTGG NP_001339703.1:n.-5-104_-5-103insTGTTGGGTGTGTTTGG
NM_001352775.2:c.-5-104_-5-103insTGTTGGGTGTGTTTGG NP_001339704.1:n.-5-104_-5-103insTGTTGGGTGTGTTTGG
NM_001352776.2:c.-8-101_-8-100insTGTTGGGTGTGTTTGG NP_001339705.1:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
NM_001352777.2:c.-8-101_-8-100insTGTTGGGTGTGTTTGG NP_001339706.1:n.-8-101_-8-100insTGTTGGGTGTGTTTGG
NM_021991.4:c.-8-101_-8-100insTGTTGGGTGTGTTTGG NP_068831.1:n.-8-101_-8-100insTGTTGGGTGTGTTTGG