Canonical Allele Identifier: CA435799600

Gene: UBA5 NPHP3-ACAD11

Linked Data

• MyVariant Identifiers: chr3:g.132390989G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.132672145G>A , CM000665.2:g.132672145G>A	GRCh38
NC_000003.11:g.132390989G>A , CM000665.1:g.132390989G>A	GRCh37
NC_000003.10:g.133873679G>A	NCBI36
NG_052968.1:g.22700G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683741.1:c.951G>A (UBA5)	ENSP00000507396.1:p.Val317=
ENST00000356232.10:c.780G>A (UBA5) MANE Select	ENSP00000348565.4:p.Val260=
ENST00000264991.8:c.612G>A (UBA5)	ENSP00000264991.4:p.Val204=
ENST00000356232.8:c.780G>A (UBA5)	ENSP00000348565.4:p.Val260=
ENST00000468227.5:n.2211G>A (UBA5)
ENST00000469158.1:n.569G>A (UBA5)
ENST00000471702.2:c.*1980+9769C>T (NPHP3-ACAD11)	ENSP00000419763.1:n.*1980+9769C>T
ENST00000473651.5:c.780G>A (UBA5)	ENSP00000424984.1:p.Val260=
ENST00000493720.6:c.780G>A (UBA5)	ENSP00000417879.2:p.Val260=
ENST00000494238.6:c.612G>A (UBA5)	ENSP00000418807.2:p.Val204=
ENST00000632629.1:c.636+9769C>T (NPHP3-ACAD11)
NM_024818.3:c.780G>A (UBA5)	NP_079094.1:p.Val260=
NM_198329.2:c.612G>A (UBA5)	NP_938143.1:p.Val204=
NR_037804.1:n.3995+9769C>T (NPHP3-ACAD11)
XM_006713752.2:c.444G>A (UBA5)	XP_006713815.1:p.Val148=
XM_011513183.1:c.639G>A (UBA5)	XP_011511485.1:p.Val213=
XM_011513184.1:c.612G>A (UBA5)	XP_011511486.1:p.Val204=
XM_011513185.1:c.510G>A (UBA5)	XP_011511487.1:p.Val170=
NM_001320210.1:c.612G>A (UBA5)	NP_001307139.1:p.Val204=
NM_001321238.1:c.510G>A (UBA5)	NP_001308167.1:p.Val170=
NM_001321239.1:c.444G>A (UBA5)	NP_001308168.1:p.Val148=
NM_024818.4:c.780G>A (UBA5)	NP_079094.1:p.Val260=
NM_198329.3:c.612G>A (UBA5)	NP_938143.1:p.Val204=
XR_001740272.1:n.1382G>A (UBA5)
NM_024818.5:c.780G>A (UBA5)	NP_079094.1:p.Val260=
NM_001320210.2:c.612G>A (UBA5)	NP_001307139.1:p.Val204=
NM_001321238.2:c.510G>A (UBA5)	NP_001308167.1:p.Val170=
NM_024818.6:c.780G>A (UBA5) MANE Select	NP_079094.1:p.Val260=
NM_198329.4:c.612G>A (UBA5)	NP_938143.1:p.Val204=