Canonical Allele Identifier: CA2260176166

Gene: JUP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41769491_41769494delinsTTGA , CM000679.2:g.41769491_41769494delinsTTGA	GRCh38
NC_000017.10:g.39925743_39925746delinsTTGA , CM000679.1:g.39925743_39925746delinsTTGA	GRCh37
NC_000017.9:g.37179269_37179272delinsTTGA	NCBI36
NG_009090.2:g.22219_22222delinsTCAA , LRG_401:g.22219_22222delinsTCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393931.8:c.392_395delinsTCAA MANE Select	ENSP00000377508.3:p.Ile131=
ENST00000310706.9:c.392_395delinsTCAA	ENSP00000311113.5:p.Ile131=
ENST00000393930.5:c.392_395delinsTCAA	ENSP00000377507.1:p.Ile131=
ENST00000393931.7:c.392_395delinsTCAA	ENSP00000377508.3:p.Ile131=
ENST00000420370.5:c.392_395delinsTCAA	ENSP00000411449.1:p.Ile131=
ENST00000424457.5:c.392_395delinsTCAA	ENSP00000401034.1:p.Ile131=
ENST00000437187.5:c.392_395delinsTCAA	ENSP00000394146.1:p.Ile131=
ENST00000449889.5:c.392_395delinsTCAA	ENSP00000389886.1:p.Ile131=
NM_002230.2:c.392_395delinsTCAA , LRG_401t2:c.392_395delinsTCAA	NP_002221.1:p.Ile131=
NM_021991.2:c.392_395delinsTCAA , LRG_401t1:c.392_395delinsTCAA	NP_068831.1:p.Ile131=
XM_006721873.1:c.392_395delinsTCAA	XP_006721936.1:p.Ile131=
XM_006721874.1:c.392_395delinsTCAA	XP_006721937.1:p.Ile131=
XM_006721875.1:c.392_395delinsTCAA	XP_006721938.1:p.Ile131=
XM_006721878.1:c.392_395delinsTCAA	XP_006721941.1:p.Ile131=
XM_011524753.1:c.392_395delinsTCAA	XP_011523055.1:p.Ile131=
XM_011524754.1:c.392_395delinsTCAA	XP_011523056.1:p.Ile131=
XM_011524755.1:c.392_395delinsTCAA	XP_011523057.1:p.Ile131=
XM_011524756.1:c.392_395delinsTCAA	XP_011523058.1:p.Ile131=
XM_011524757.1:c.392_395delinsTCAA	XP_011523059.1:p.Ile131=
XM_011524758.1:c.392_395delinsTCAA	XP_011523060.1:p.Ile131=
NM_001352773.1:c.392_395delinsTCAA	NP_001339702.1:p.Ile131=
NM_001352774.1:c.392_395delinsTCAA	NP_001339703.1:p.Ile131=
NM_001352775.1:c.392_395delinsTCAA	NP_001339704.1:p.Ile131=
NM_001352776.1:c.392_395delinsTCAA	NP_001339705.1:p.Ile131=
NM_001352777.1:c.392_395delinsTCAA	NP_001339706.1:p.Ile131=
NM_002230.3:c.392_395delinsTCAA	NP_002221.1:p.Ile131=
NM_021991.3:c.392_395delinsTCAA	NP_068831.1:p.Ile131=
XM_006721874.3:c.392_395delinsTCAA	XP_006721937.1:p.Ile131=
XM_011524753.2:c.392_395delinsTCAA	XP_011523055.1:p.Ile131=
XM_017024588.2:c.443_446delinsTCAA	XP_016880077.1:p.Ile148=
XM_017024590.1:c.392_395delinsTCAA	XP_016880079.1:p.Ile131=
NM_002230.4:c.392_395delinsTCAA MANE Select	NP_002221.1:p.Ile131=
NM_001352773.2:c.392_395delinsTCAA	NP_001339702.1:p.Ile131=
NM_001352774.2:c.392_395delinsTCAA	NP_001339703.1:p.Ile131=
NM_001352775.2:c.392_395delinsTCAA	NP_001339704.1:p.Ile131=
NM_001352776.2:c.392_395delinsTCAA	NP_001339705.1:p.Ile131=
NM_001352777.2:c.392_395delinsTCAA	NP_001339706.1:p.Ile131=
NM_021991.4:c.392_395delinsTCAA	NP_068831.1:p.Ile131=