Canonical Allele Identifier: CA2809501009

Gene: JUP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41755534_41755535del , CM000679.2:g.41755534_41755535del	GRCh38
NC_000017.10:g.39911786_39911787del , CM000679.1:g.39911786_39911787del	GRCh37
NC_000017.9:g.37165312_37165313del	NCBI36
NG_009090.2:g.36180_36181del , LRG_401:g.36180_36181del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393931.8:c.*211_*212del MANE Select	ENSP00000377508.3:n.*211_*212del
ENST00000310706.9:c.*15-101_*15-100del	ENSP00000311113.5:n.*15-101_*15-100del
ENST00000393930.5:c.*15-101_*15-100del	ENSP00000377507.1:n.*15-101_*15-100del
ENST00000393931.7:c.*211_*212del	ENSP00000377508.3:n.*211_*212del
NM_002230.2:c.*211_*212del , LRG_401t2:c.*211_*212del	NP_002221.1:n.*211_*212del
NM_021991.2:c.*15-101_*15-100del , LRG_401t1:c.*15-101_*15-100del	NP_068831.1:n.*15-101_*15-100del
XM_006721873.1:c.*15-101_*15-100del	XP_006721936.1:n.*15-101_*15-100del
XM_006721874.1:c.*15-101_*15-100del	XP_006721937.1:n.*15-101_*15-100del
XM_006721875.1:c.*15-101_*15-100del	XP_006721938.1:n.*15-101_*15-100del
XM_006721878.1:c.*15-101_*15-100del	XP_006721941.1:n.*15-101_*15-100del
XM_011524753.1:c.*15-101_*15-100del	XP_011523055.1:n.*15-101_*15-100del
XM_011524754.1:c.*15-101_*15-100del	XP_011523056.1:n.*15-101_*15-100del
XM_011524755.1:c.*15-101_*15-100del	XP_011523057.1:n.*15-101_*15-100del
XM_011524756.1:c.*15-101_*15-100del	XP_011523058.1:n.*15-101_*15-100del
XM_011524757.1:c.*15-101_*15-100del	XP_011523059.1:n.*15-101_*15-100del
XM_011524758.1:c.*15-101_*15-100del	XP_011523060.1:n.*15-101_*15-100del
NM_001352773.1:c.*211_*212del	NP_001339702.1:n.*211_*212del
NM_001352774.1:c.*15-101_*15-100del	NP_001339703.1:n.*15-101_*15-100del
NM_001352775.1:c.*15-101_*15-100del	NP_001339704.1:n.*15-101_*15-100del
NM_001352776.1:c.*15-101_*15-100del	NP_001339705.1:n.*15-101_*15-100del
NM_001352777.1:c.*15-101_*15-100del	NP_001339706.1:n.*15-101_*15-100del
NM_002230.3:c.*211_*212del	NP_002221.1:n.*211_*212del
NM_021991.3:c.*15-101_*15-100del	NP_068831.1:n.*15-101_*15-100del
XM_006721874.3:c.*15-101_*15-100del	XP_006721937.1:n.*15-101_*15-100del
XM_011524753.2:c.*15-101_*15-100del	XP_011523055.1:n.*15-101_*15-100del
XM_017024588.2:c.*15-101_*15-100del	XP_016880077.1:n.*15-101_*15-100del
XM_017024590.1:c.*15-101_*15-100del	XP_016880079.1:n.*15-101_*15-100del
NM_002230.4:c.*211_*212del MANE Select	NP_002221.1:n.*211_*212del
NM_001352773.2:c.*211_*212del	NP_001339702.1:n.*211_*212del
NM_001352774.2:c.*15-101_*15-100del	NP_001339703.1:n.*15-101_*15-100del
NM_001352775.2:c.*15-101_*15-100del	NP_001339704.1:n.*15-101_*15-100del
NM_001352776.2:c.*15-101_*15-100del	NP_001339705.1:n.*15-101_*15-100del
NM_001352777.2:c.*15-101_*15-100del	NP_001339706.1:n.*15-101_*15-100del
NM_021991.4:c.*15-101_*15-100del	NP_068831.1:n.*15-101_*15-100del