Canonical Allele Identifier: CA382116833

Gene: ALG8

Linked Data

• ClinVar Variation Id: 1372613
• ClinVar RCV Id: RCV001908065 ; RCV002506931
• dbSNP Id: rs1860433537
• MyVariant Identifiers: chr11:g.77824937C>T (hg19) ; chr11:g.78113891C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.78113891C>T , CM000673.2:g.78113891C>T	GRCh38
NC_000011.9:g.77824937C>T , CM000673.1:g.77824937C>T	GRCh37
NC_000011.8:g.77502585C>T	NCBI36
NG_008926.1:g.30763G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299626.10:c.772G>A MANE Select	ENSP00000299626.5:p.Ala258Thr
ENST00000524925.2:n.884G>A
ENST00000525755.6:c.*404G>A	ENSP00000435467.2:n.*404G>A
ENST00000525761.3:c.508G>A	ENSP00000431357.3:p.Ala170Thr
ENST00000525783.6:c.508G>A	ENSP00000434066.2:p.Ala170Thr
ENST00000525870.6:c.772G>A	ENSP00000435417.2:p.Ala258Thr
ENST00000526737.6:c.*303G>A	ENSP00000436366.2:n.*303G>A
ENST00000526849.6:c.676G>A	ENSP00000434388.2:p.Ala226Thr
ENST00000527099.2:c.508G>A	ENSP00000436064.2:p.Ala170Thr
ENST00000529139.6:c.772G>A	ENSP00000432953.2:p.Ala258Thr
ENST00000530454.6:c.772G>A	ENSP00000434660.2:p.Ala258Thr
ENST00000530608.6:c.571G>A	ENSP00000432381.2:p.Ala191Thr
ENST00000530910.6:c.508G>A	ENSP00000437033.2:p.Ala170Thr
ENST00000532306.6:c.772G>A	ENSP00000435626.2:p.Ala258Thr
ENST00000532440.6:c.772G>A	ENSP00000433429.2:p.Ala258Thr
ENST00000615266.5:c.772G>A	ENSP00000480742.2:p.Ala258Thr
ENST00000679444.1:c.508G>A	ENSP00000506099.1:p.Ala170Thr
ENST00000679497.1:c.508G>A	ENSP00000505407.1:p.Ala170Thr
ENST00000679539.1:c.772G>A	ENSP00000504910.1:p.Ala258Thr
ENST00000679559.1:c.772G>A	ENSP00000505433.1:p.Ala258Thr
ENST00000679581.1:n.1508G>A
ENST00000679648.1:c.*303G>A	ENSP00000505726.1:n.*303G>A
ENST00000679685.1:c.*156G>A	ENSP00000505698.1:n.*156G>A
ENST00000679697.1:c.772G>A	ENSP00000505696.1:p.Ala258Thr
ENST00000679874.1:c.*303G>A	ENSP00000506314.1:n.*303G>A
ENST00000679986.1:c.*303G>A	ENSP00000505614.1:n.*303G>A
ENST00000680063.1:c.*303G>A	ENSP00000504928.1:n.*303G>A
ENST00000680101.1:c.508G>A	ENSP00000504917.1:p.Ala170Thr
ENST00000680142.1:n.905-6979G>A
ENST00000680223.1:c.772G>A	ENSP00000505023.1:p.Ala258Thr
ENST00000680256.1:c.775G>A	ENSP00000505074.1:p.Ala259Thr
ENST00000680329.1:c.508G>A	ENSP00000506215.1:p.Ala170Thr
ENST00000680398.1:c.772G>A	ENSP00000506189.1:p.Ala258Thr
ENST00000680399.1:c.772G>A	ENSP00000505984.1:p.Ala258Thr
ENST00000680459.1:c.*395G>A	ENSP00000506617.1:n.*395G>A
ENST00000680467.1:c.772G>A	ENSP00000505609.1:p.Ala258Thr
ENST00000680499.1:c.508G>A	ENSP00000506092.1:p.Ala170Thr
ENST00000680580.1:c.508G>A	ENSP00000506170.1:p.Ala170Thr
ENST00000680643.1:c.772G>A	ENSP00000505207.1:p.Ala258Thr
ENST00000680761.1:c.508G>A	ENSP00000506421.1:p.Ala170Thr
ENST00000680797.1:c.*303G>A	ENSP00000506717.1:n.*303G>A
ENST00000680829.1:c.508G>A	ENSP00000506408.1:p.Ala170Thr
ENST00000680866.1:c.772G>A	ENSP00000505649.1:p.Ala258Thr
ENST00000680996.1:c.508G>A	ENSP00000505468.1:p.Ala170Thr
ENST00000681221.1:c.508G>A	ENSP00000505136.1:p.Ala170Thr
ENST00000681225.1:c.508G>A	ENSP00000505016.1:p.Ala170Thr
ENST00000681351.1:c.508G>A	ENSP00000506652.1:p.Ala170Thr
ENST00000681384.1:c.508G>A	ENSP00000506249.1:p.Ala170Thr
ENST00000681417.1:c.508G>A	ENSP00000505965.1:p.Ala170Thr
ENST00000681489.1:c.508G>A	ENSP00000505200.1:p.Ala170Thr
ENST00000681575.1:c.508G>A	ENSP00000505743.1:p.Ala170Thr
ENST00000681699.1:c.601G>A	ENSP00000504969.1:p.Ala201Thr
ENST00000681723.1:c.508G>A	ENSP00000506059.1:p.Ala170Thr
ENST00000681765.1:c.508G>A	ENSP00000505811.1:p.Ala170Thr
ENST00000681853.1:n.1466G>A
ENST00000681957.1:c.772G>A	ENSP00000506056.1:p.Ala258Thr
ENST00000299626.9:c.772G>A	ENSP00000299626.5:p.Ala258Thr
ENST00000376156.7:c.772G>A	ENSP00000365326.3:p.Ala258Thr
ENST00000524925.1:n.210G>A
ENST00000525755.5:c.619G>A	ENSP00000435467.1:p.Ala207Thr
ENST00000525870.5:c.508G>A	ENSP00000435417.1:p.Ala170Thr
ENST00000526737.5:c.*404G>A	ENSP00000436366.1:n.*404G>A
ENST00000529139.5:c.306G>A
ENST00000530454.5:c.775G>A	ENSP00000434660.1:p.Ala259Thr
ENST00000530608.5:c.51G>A
ENST00000532306.5:c.393G>A
ENST00000532440.5:c.226G>A	ENSP00000433429.1:p.Ala76Thr
ENST00000532552.2:n.122-4310G>A
ENST00000615266.4:c.772G>A	ENSP00000480742.1:p.Ala258Thr
NM_001007027.2:c.772G>A	NP_001007028.1:p.Ala258Thr
NM_024079.4:c.772G>A	NP_076984.2:p.Ala258Thr
XM_005274247.2:c.745G>A	XP_005274304.1:p.Ala249Thr
XM_011545251.1:c.772G>A	XP_011543553.1:p.Ala258Thr
XM_011545252.1:c.508G>A	XP_011543554.1:p.Ala170Thr
XR_428923.2:n.844G>A
XR_950044.1:n.844G>A
XR_950045.1:n.844G>A
XM_005274247.3:c.745G>A	XP_005274304.1:p.Ala249Thr
XM_011545252.2:c.508G>A	XP_011543554.1:p.Ala170Thr
XM_017018274.1:c.745G>A	XP_016873763.1:p.Ala249Thr
XR_001747956.1:n.1594G>A
XR_428923.4:n.827G>A
XR_950044.3:n.827G>A
XR_950045.3:n.827G>A
NM_024079.5:c.772G>A MANE Select	NP_076984.2:p.Ala258Thr
NM_001007027.3:c.772G>A	NP_001007028.1:p.Ala258Thr