Canonical Allele Identifier: CA1321181876
Gene: ALS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201723391C= , CM000664.2:g.201723391C= GRCh38
NC_000002.11:g.202588114C= , CM000664.1:g.202588114C= GRCh37
NC_000002.10:g.202296359C= NCBI36
NG_008775.1:g.62782G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264276.11:c.3563G= MANE Select ENSP00000264276.6:p.Gly1188=
ENST00000439495.6:c.1241G= ENSP00000403832.2:p.Gly414=
ENST00000482891.6:n.4331G=
ENST00000494017.6:n.1295G=
ENST00000679409.1:c.1241G= ENSP00000506531.1:p.Gly414=
ENST00000679416.1:n.5067G=
ENST00000679435.1:c.3563G= ENSP00000505218.1:p.Gly1188=
ENST00000679516.1:c.3563G= ENSP00000505187.1:p.Gly1188=
ENST00000679618.1:c.*651G= ENSP00000506274.1:n.*651G=
ENST00000679630.1:n.5412G=
ENST00000679686.1:n.3677G=
ENST00000679701.1:n.6555G=
ENST00000679916.1:c.3563G= ENSP00000506172.1:p.Gly1188=
ENST00000680000.1:c.3563G= ENSP00000506173.1:p.Gly1188=
ENST00000680135.1:c.*1527G= ENSP00000506211.1:n.*1527G=
ENST00000680149.1:c.3563G= ENSP00000506497.1:p.Gly1188=
ENST00000680163.1:c.3563G= ENSP00000505092.1:p.Gly1188=
ENST00000680174.1:n.4254G=
ENST00000680236.1:c.*624G= ENSP00000506212.1:n.*624G=
ENST00000680497.1:c.3665G= ENSP00000505954.1:p.Gly1222=
ENST00000680508.1:c.3563G= ENSP00000505749.1:p.Gly1188=
ENST00000680569.1:c.*1274G= ENSP00000505522.1:n.*1274G=
ENST00000680630.1:n.3995G=
ENST00000680634.1:n.21-2902G=
ENST00000680722.1:n.1363G=
ENST00000680723.1:n.4346G=
ENST00000680726.1:c.3563G= ENSP00000505505.1:p.Gly1188=
ENST00000680737.1:n.3834G=
ENST00000680759.1:c.3563G= ENSP00000505848.1:p.Gly1188=
ENST00000680814.1:c.3563G= ENSP00000505710.1:p.Gly1188=
ENST00000680828.1:c.*1135G= ENSP00000505249.1:n.*1135G=
ENST00000680861.1:c.3563G= ENSP00000505043.1:p.Gly1188=
ENST00000680927.1:c.3563G= ENSP00000505473.1:p.Gly1188=
ENST00000680939.1:n.3905G=
ENST00000681152.1:c.3563G= ENSP00000505388.1:p.Gly1188=
ENST00000681250.1:c.*280G= ENSP00000505684.1:n.*280G=
ENST00000681256.1:c.*1581G= ENSP00000505446.1:n.*1581G=
ENST00000681279.1:n.4331G=
ENST00000681303.1:c.3563G= ENSP00000505576.1:p.Gly1188=
ENST00000681307.1:n.4676G=
ENST00000681461.1:n.4331G=
ENST00000681495.1:c.1103G= ENSP00000506085.1:p.Gly368=
ENST00000681558.1:c.1241G= ENSP00000505568.1:p.Gly414=
ENST00000681619.1:c.3563G= ENSP00000505071.1:p.Gly1188=
ENST00000681716.1:c.*1274G= ENSP00000505078.1:n.*1274G=
ENST00000681758.1:n.3905G=
ENST00000681768.1:c.*1227G= ENSP00000506311.1:n.*1227G=
ENST00000681808.1:c.3563G= ENSP00000505219.1:p.Gly1188=
ENST00000264276.10:c.3563G= ENSP00000264276.6:p.Gly1188=
ENST00000439495.5:c.1524G=
ENST00000482891.5:n.3703G=
ENST00000489440.5:n.384G=
NM_020919.3:c.3563G= NP_065970.2:p.Gly1188=
XM_005246709.2:c.3563G= XP_005246766.1:p.Gly1188=
XM_006712654.1:c.3563G= XP_006712717.1:p.Gly1188=
XM_006712655.2:c.1499G= XP_006712718.1:p.Gly500=
XM_011511530.1:c.3224G= XP_011509832.1:p.Gly1075=
XM_011511531.1:c.3563G= XP_011509833.1:p.Gly1188=
XR_922974.1:n.3698G=
XM_006712654.3:c.3563G= XP_006712717.1:p.Gly1188=
XM_006712655.3:c.1499G= XP_006712718.1:p.Gly500=
XM_017004569.2:c.3563G= XP_016860058.1:p.Gly1188=
XM_017004570.2:c.3563G= XP_016860059.1:p.Gly1188=
XM_017004572.2:c.1181G= XP_016860061.1:p.Gly394=
XM_024453024.1:c.3224G= XP_024308792.1:p.Gly1075=
XM_024453025.1:c.1499G= XP_024308793.1:p.Gly500=
XR_001738864.2:n.3698G=
XR_001738865.2:n.3698G=
XR_001738866.2:n.3698G=
XR_001738867.2:n.3698G=
XR_002959320.1:n.2754G=
NM_020919.4:c.3563G= MANE Select NP_065970.2:p.Gly1188=