Canonical Allele Identifier: CA772062678

Gene: JUP

Linked Data

• dbSNP Id: rs1234920327
• gnomAD v3: 17-41758822-CATGGTTGGCTGGGCACAGGGCCAGATTCCTGATCAAGCCG-C
• gnomAD v4: 17-41758822-CATGGTTGGCTGGGCACAGGGCCAGATTCCTGATCAAGCCG-C
• MyVariant Identifiers: chr17:g.41758823_41758862del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41758830_41758869del , CM000679.2:g.41758830_41758869del	GRCh38
NC_000017.10:g.39915082_39915121del , CM000679.1:g.39915082_39915121del	GRCh37
NC_000017.9:g.37168608_37168647del	NCBI36
NG_009090.2:g.32851_32890del , LRG_401:g.32851_32890del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393931.8:c.1506_1545del MANE Select	ENSP00000377508.3:p.Ile502MetfsTer18
ENST00000310706.9:c.1506_1545del	ENSP00000311113.5:p.Ile502MetfsTer18
ENST00000393930.5:c.1506_1545del	ENSP00000377507.1:p.Ile502MetfsTer18
ENST00000393931.7:c.1506_1545del	ENSP00000377508.3:p.Ile502MetfsTer18
ENST00000585793.1:n.104_143del
NM_002230.2:c.1506_1545del , LRG_401t2:c.1506_1545del	NP_002221.1:p.Ile502MetfsTer18
NM_021991.2:c.1506_1545del , LRG_401t1:c.1506_1545del	NP_068831.1:p.Ile502MetfsTer18
XM_006721873.1:c.1506_1545del	XP_006721936.1:p.Ile502MetfsTer18
XM_006721874.1:c.1506_1545del	XP_006721937.1:p.Ile502MetfsTer18
XM_006721875.1:c.1506_1545del	XP_006721938.1:p.Ile502MetfsTer18
XM_006721878.1:c.1506_1545del	XP_006721941.1:p.Ile502MetfsTer18
XM_011524753.1:c.1506_1545del	XP_011523055.1:p.Ile502MetfsTer18
XM_011524754.1:c.1506_1545del	XP_011523056.1:p.Ile502MetfsTer18
XM_011524755.1:c.1506_1545del	XP_011523057.1:p.Ile502MetfsTer18
XM_011524756.1:c.1506_1545del	XP_011523058.1:p.Ile502MetfsTer18
XM_011524757.1:c.1506_1545del	XP_011523059.1:p.Ile502MetfsTer18
XM_011524758.1:c.1506_1545del	XP_011523060.1:p.Ile502MetfsTer18
NM_001352773.1:c.1506_1545del	NP_001339702.1:p.Ile502MetfsTer18
NM_001352774.1:c.1506_1545del	NP_001339703.1:p.Ile502MetfsTer18
NM_001352775.1:c.1506_1545del	NP_001339704.1:p.Ile502MetfsTer18
NM_001352776.1:c.1506_1545del	NP_001339705.1:p.Ile502MetfsTer18
NM_001352777.1:c.1506_1545del	NP_001339706.1:p.Ile502MetfsTer18
NM_002230.3:c.1506_1545del	NP_002221.1:p.Ile502MetfsTer18
NM_021991.3:c.1506_1545del	NP_068831.1:p.Ile502MetfsTer18
XM_006721874.3:c.1506_1545del	XP_006721937.1:p.Ile502MetfsTer18
XM_011524753.2:c.1506_1545del	XP_011523055.1:p.Ile502MetfsTer18
XM_017024588.2:c.1557_1596del	XP_016880077.1:p.Ile519MetfsTer18
XM_017024590.1:c.1506_1545del	XP_016880079.1:p.Ile502MetfsTer18
NM_002230.4:c.1506_1545del MANE Select	NP_002221.1:p.Ile502MetfsTer18
NM_001352773.2:c.1506_1545del	NP_001339702.1:p.Ile502MetfsTer18
NM_001352774.2:c.1506_1545del	NP_001339703.1:p.Ile502MetfsTer18
NM_001352775.2:c.1506_1545del	NP_001339704.1:p.Ile502MetfsTer18
NM_001352776.2:c.1506_1545del	NP_001339705.1:p.Ile502MetfsTer18
NM_001352777.2:c.1506_1545del	NP_001339706.1:p.Ile502MetfsTer18
NM_021991.4:c.1506_1545del	NP_068831.1:p.Ile502MetfsTer18