Canonical Allele Identifier: CA1321181947
Gene: ALS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201723436_201723437delinsTC , CM000664.2:g.201723436_201723437delinsTC GRCh38
NC_000002.11:g.202588159_202588160delinsTC , CM000664.1:g.202588159_202588160delinsTC GRCh37
NC_000002.10:g.202296404_202296405delinsTC NCBI36
NG_008775.1:g.62736_62737delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000264276.11:c.3517_3518delinsGA MANE Select ENSP00000264276.6:p.Glu1173=
ENST00000439495.6:c.1195_1196delinsGA ENSP00000403832.2:p.Glu399=
ENST00000482891.6:n.4285_4286delinsGA
ENST00000494017.6:n.1249_1250delinsGA
ENST00000679409.1:c.1195_1196delinsGA ENSP00000506531.1:p.Glu399=
ENST00000679416.1:n.5021_5022delinsGA
ENST00000679435.1:c.3517_3518delinsGA ENSP00000505218.1:p.Glu1173=
ENST00000679516.1:c.3517_3518delinsGA ENSP00000505187.1:p.Glu1173=
ENST00000679618.1:c.*605_*606delinsGA ENSP00000506274.1:n.*605_*606delinsGA
ENST00000679630.1:n.5366_5367delinsGA
ENST00000679686.1:n.3631_3632delinsGA
ENST00000679701.1:n.6509_6510delinsGA
ENST00000679916.1:c.3517_3518delinsGA ENSP00000506172.1:p.Glu1173=
ENST00000680000.1:c.3517_3518delinsGA ENSP00000506173.1:p.Glu1173=
ENST00000680135.1:c.*1481_*1482delinsGA ENSP00000506211.1:n.*1481_*1482delinsGA
ENST00000680149.1:c.3517_3518delinsGA ENSP00000506497.1:p.Glu1173=
ENST00000680163.1:c.3517_3518delinsGA ENSP00000505092.1:p.Glu1173=
ENST00000680174.1:n.4208_4209delinsGA
ENST00000680236.1:c.*578_*579delinsGA ENSP00000506212.1:n.*578_*579delinsGA
ENST00000680497.1:c.3619_3620delinsGA ENSP00000505954.1:p.Glu1207=
ENST00000680508.1:c.3517_3518delinsGA ENSP00000505749.1:p.Glu1173=
ENST00000680569.1:c.*1228_*1229delinsGA ENSP00000505522.1:n.*1228_*1229delinsGA
ENST00000680630.1:n.3949_3950delinsGA
ENST00000680634.1:n.21-2948_21-2947delinsGA
ENST00000680722.1:n.1317_1318delinsGA
ENST00000680723.1:n.4300_4301delinsGA
ENST00000680726.1:c.3517_3518delinsGA ENSP00000505505.1:p.Glu1173=
ENST00000680737.1:n.3788_3789delinsGA
ENST00000680759.1:c.3517_3518delinsGA ENSP00000505848.1:p.Glu1173=
ENST00000680814.1:c.3517_3518delinsGA ENSP00000505710.1:p.Glu1173=
ENST00000680828.1:c.*1089_*1090delinsGA ENSP00000505249.1:n.*1089_*1090delinsGA
ENST00000680861.1:c.3517_3518delinsGA ENSP00000505043.1:p.Glu1173=
ENST00000680927.1:c.3517_3518delinsGA ENSP00000505473.1:p.Glu1173=
ENST00000680939.1:n.3859_3860delinsGA
ENST00000681152.1:c.3517_3518delinsGA ENSP00000505388.1:p.Glu1173=
ENST00000681250.1:c.*234_*235delinsGA ENSP00000505684.1:n.*234_*235delinsGA
ENST00000681256.1:c.*1535_*1536delinsGA ENSP00000505446.1:n.*1535_*1536delinsGA
ENST00000681279.1:n.4285_4286delinsGA
ENST00000681303.1:c.3517_3518delinsGA ENSP00000505576.1:p.Glu1173=
ENST00000681307.1:n.4630_4631delinsGA
ENST00000681461.1:n.4285_4286delinsGA
ENST00000681495.1:c.1057_1058delinsGA ENSP00000506085.1:p.Glu353=
ENST00000681558.1:c.1195_1196delinsGA ENSP00000505568.1:p.Glu399=
ENST00000681619.1:c.3517_3518delinsGA ENSP00000505071.1:p.Glu1173=
ENST00000681716.1:c.*1228_*1229delinsGA ENSP00000505078.1:n.*1228_*1229delinsGA
ENST00000681758.1:n.3859_3860delinsGA
ENST00000681768.1:c.*1181_*1182delinsGA ENSP00000506311.1:n.*1181_*1182delinsGA
ENST00000681808.1:c.3517_3518delinsGA ENSP00000505219.1:p.Glu1173=
ENST00000264276.10:c.3517_3518delinsGA ENSP00000264276.6:p.Glu1173=
ENST00000439495.5:c.1478_1479delinsGA
ENST00000482891.5:n.3657_3658delinsGA
ENST00000489440.5:n.338_339delinsGA
NM_020919.3:c.3517_3518delinsGA NP_065970.2:p.Glu1173=
XM_005246709.2:c.3517_3518delinsGA XP_005246766.1:p.Glu1173=
XM_006712654.1:c.3517_3518delinsGA XP_006712717.1:p.Glu1173=
XM_006712655.2:c.1453_1454delinsGA XP_006712718.1:p.Glu485=
XM_011511530.1:c.3178_3179delinsGA XP_011509832.1:p.Glu1060=
XM_011511531.1:c.3517_3518delinsGA XP_011509833.1:p.Glu1173=
XR_922974.1:n.3652_3653delinsGA
XM_006712654.3:c.3517_3518delinsGA XP_006712717.1:p.Glu1173=
XM_006712655.3:c.1453_1454delinsGA XP_006712718.1:p.Glu485=
XM_017004569.2:c.3517_3518delinsGA XP_016860058.1:p.Glu1173=
XM_017004570.2:c.3517_3518delinsGA XP_016860059.1:p.Glu1173=
XM_017004572.2:c.1135_1136delinsGA XP_016860061.1:p.Glu379=
XM_024453024.1:c.3178_3179delinsGA XP_024308792.1:p.Glu1060=
XM_024453025.1:c.1453_1454delinsGA XP_024308793.1:p.Glu485=
XR_001738864.2:n.3652_3653delinsGA
XR_001738865.2:n.3652_3653delinsGA
XR_001738866.2:n.3652_3653delinsGA
XR_001738867.2:n.3652_3653delinsGA
XR_002959320.1:n.2708_2709delinsGA
NM_020919.4:c.3517_3518delinsGA MANE Select NP_065970.2:p.Glu1173=