Canonical Allele Identifier: CA399501499

Gene: JUP

Linked Data

• MyVariant Identifiers: chr17:g.39923785T>G (hg19) ; chr17:g.41767533T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41767533T>G , CM000679.2:g.41767533T>G	GRCh38
NC_000017.10:g.39923785T>G , CM000679.1:g.39923785T>G	GRCh37
NC_000017.9:g.37177311T>G	NCBI36
NG_009090.2:g.24180A>C , LRG_401:g.24180A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393931.8:c.755A>C MANE Select	ENSP00000377508.3:p.Asn252Thr
ENST00000310706.9:c.755A>C	ENSP00000311113.5:p.Asn252Thr
ENST00000393930.5:c.755A>C	ENSP00000377507.1:p.Asn252Thr
ENST00000393931.7:c.755A>C	ENSP00000377508.3:p.Asn252Thr
ENST00000420370.5:c.755A>C	ENSP00000411449.1:p.Asn252Thr
ENST00000437187.5:c.755A>C	ENSP00000394146.1:p.Asn252Thr
ENST00000449889.5:c.755A>C	ENSP00000389886.1:p.Asn252Thr
NM_002230.2:c.755A>C , LRG_401t2:c.755A>C	NP_002221.1:p.Asn252Thr
NM_021991.2:c.755A>C , LRG_401t1:c.755A>C	NP_068831.1:p.Asn252Thr
XM_006721873.1:c.755A>C	XP_006721936.1:p.Asn252Thr
XM_006721874.1:c.755A>C	XP_006721937.1:p.Asn252Thr
XM_006721875.1:c.755A>C	XP_006721938.1:p.Asn252Thr
XM_006721878.1:c.755A>C	XP_006721941.1:p.Asn252Thr
XM_011524753.1:c.755A>C	XP_011523055.1:p.Asn252Thr
XM_011524754.1:c.755A>C	XP_011523056.1:p.Asn252Thr
XM_011524755.1:c.755A>C	XP_011523057.1:p.Asn252Thr
XM_011524756.1:c.755A>C	XP_011523058.1:p.Asn252Thr
XM_011524757.1:c.755A>C	XP_011523059.1:p.Asn252Thr
XM_011524758.1:c.755A>C	XP_011523060.1:p.Asn252Thr
NM_001352773.1:c.755A>C	NP_001339702.1:p.Asn252Thr
NM_001352774.1:c.755A>C	NP_001339703.1:p.Asn252Thr
NM_001352775.1:c.755A>C	NP_001339704.1:p.Asn252Thr
NM_001352776.1:c.755A>C	NP_001339705.1:p.Asn252Thr
NM_001352777.1:c.755A>C	NP_001339706.1:p.Asn252Thr
NM_002230.3:c.755A>C	NP_002221.1:p.Asn252Thr
NM_021991.3:c.755A>C	NP_068831.1:p.Asn252Thr
XM_006721874.3:c.755A>C	XP_006721937.1:p.Asn252Thr
XM_011524753.2:c.755A>C	XP_011523055.1:p.Asn252Thr
XM_017024588.2:c.806A>C	XP_016880077.1:p.Asn269Thr
XM_017024590.1:c.755A>C	XP_016880079.1:p.Asn252Thr
NM_002230.4:c.755A>C MANE Select	NP_002221.1:p.Asn252Thr
NM_001352773.2:c.755A>C	NP_001339702.1:p.Asn252Thr
NM_001352774.2:c.755A>C	NP_001339703.1:p.Asn252Thr
NM_001352775.2:c.755A>C	NP_001339704.1:p.Asn252Thr
NM_001352776.2:c.755A>C	NP_001339705.1:p.Asn252Thr
NM_001352777.2:c.755A>C	NP_001339706.1:p.Asn252Thr
NM_021991.4:c.755A>C	NP_068831.1:p.Asn252Thr