Canonical Allele Identifier: CA2637858116

Gene: JUP

Linked Data

• gnomAD v4: 17-41756007-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41756007_41756008insT , CM000679.2:g.41756007_41756008insT	GRCh38
NC_000017.10:g.39912259_39912260insT , CM000679.1:g.39912259_39912260insT	GRCh37
NC_000017.9:g.37165785_37165786insT	NCBI36
NG_009090.2:g.35705_35706insA , LRG_401:g.35705_35706insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000393931.8:c.2087-113_2087-112insA MANE Select	ENSP00000377508.3:n.2087-113_2087-112insA...
ENST00000310706.9:c.2087-113_2087-112insA	ENSP00000311113.5:n.2087-113_2087-112insA...
ENST00000393930.5:c.2087-113_2087-112insA	ENSP00000377507.1:n.2087-113_2087-112insA...
ENST00000393931.7:c.2087-113_2087-112insA	ENSP00000377508.3:n.2087-113_2087-112insA...
NM_002230.2:c.2087-113_2087-112insA , LRG_401t2:c.2087-113_2087-112insA	NP_002221.1:n.2087-113_2087-112insA
NM_021991.2:c.2087-113_2087-112insA , LRG_401t1:c.2087-113_2087-112insA	NP_068831.1:n.2087-113_2087-112insA
XM_006721873.1:c.2087-113_2087-112insA	XP_006721936.1:n.2087-113_2087-112insA
XM_006721874.1:c.2087-113_2087-112insA	XP_006721937.1:n.2087-113_2087-112insA
XM_006721875.1:c.2087-113_2087-112insA	XP_006721938.1:n.2087-113_2087-112insA
XM_006721878.1:c.2087-113_2087-112insA	XP_006721941.1:n.2087-113_2087-112insA
XM_011524753.1:c.2087-113_2087-112insA	XP_011523055.1:n.2087-113_2087-112insA
XM_011524754.1:c.2087-113_2087-112insA	XP_011523056.1:n.2087-113_2087-112insA
XM_011524755.1:c.2087-113_2087-112insA	XP_011523057.1:n.2087-113_2087-112insA
XM_011524756.1:c.2087-113_2087-112insA	XP_011523058.1:n.2087-113_2087-112insA
XM_011524757.1:c.2087-113_2087-112insA	XP_011523059.1:n.2087-113_2087-112insA
XM_011524758.1:c.2087-113_2087-112insA	XP_011523060.1:n.2087-113_2087-112insA
NM_001352773.1:c.2087-113_2087-112insA	NP_001339702.1:n.2087-113_2087-112insA
NM_001352774.1:c.2087-113_2087-112insA	NP_001339703.1:n.2087-113_2087-112insA
NM_001352775.1:c.2087-113_2087-112insA	NP_001339704.1:n.2087-113_2087-112insA
NM_001352776.1:c.2087-113_2087-112insA	NP_001339705.1:n.2087-113_2087-112insA
NM_001352777.1:c.2087-113_2087-112insA	NP_001339706.1:n.2087-113_2087-112insA
NM_002230.3:c.2087-113_2087-112insA	NP_002221.1:n.2087-113_2087-112insA
NM_021991.3:c.2087-113_2087-112insA	NP_068831.1:n.2087-113_2087-112insA
XM_006721874.3:c.2087-113_2087-112insA	XP_006721937.1:n.2087-113_2087-112insA
XM_011524753.2:c.2087-113_2087-112insA	XP_011523055.1:n.2087-113_2087-112insA
XM_017024588.2:c.2138-113_2138-112insA	XP_016880077.1:n.2138-113_2138-112insA
XM_017024590.1:c.2087-113_2087-112insA	XP_016880079.1:n.2087-113_2087-112insA
NM_002230.4:c.2087-113_2087-112insA MANE Select	NP_002221.1:n.2087-113_2087-112insA
NM_001352773.2:c.2087-113_2087-112insA	NP_001339702.1:n.2087-113_2087-112insA
NM_001352774.2:c.2087-113_2087-112insA	NP_001339703.1:n.2087-113_2087-112insA
NM_001352775.2:c.2087-113_2087-112insA	NP_001339704.1:n.2087-113_2087-112insA
NM_001352776.2:c.2087-113_2087-112insA	NP_001339705.1:n.2087-113_2087-112insA
NM_001352777.2:c.2087-113_2087-112insA	NP_001339706.1:n.2087-113_2087-112insA
NM_021991.4:c.2087-113_2087-112insA	NP_068831.1:n.2087-113_2087-112insA