Canonical Allele Identifier: CA63936943
Gene: ALS2 HGNC NCBI

Linked Data

dbSNP Id: rs74267265

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201722993T>A , CM000664.2:g.201722993T>A GRCh38
NC_000002.11:g.202587716T>A , CM000664.1:g.202587716T>A GRCh37
NC_000002.10:g.202295961T>A NCBI36
NG_008775.1:g.63180A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264276.11:c.3702+50A>T MANE Select ENSP00000264276.6:n.3702+50A>T
ENST00000439495.6:c.1380+50A>T ENSP00000403832.2:n.1380+50A>T
ENST00000482891.6:n.4520A>T
ENST00000494017.6:n.1484A>T
ENST00000679409.1:c.1380+50A>T ENSP00000506531.1:n.1380+50A>T
ENST00000679416.1:n.5206+50A>T
ENST00000679435.1:c.3702+50A>T ENSP00000505218.1:n.3702+50A>T
ENST00000679516.1:c.3702+50A>T ENSP00000505187.1:n.3702+50A>T
ENST00000679618.1:c.*790+50A>T ENSP00000506274.1:n.*790+50A>T
ENST00000679630.1:n.5551+50A>T
ENST00000679686.1:n.3816+50A>T
ENST00000679701.1:n.6694+50A>T
ENST00000679916.1:c.3702+50A>T ENSP00000506172.1:n.3702+50A>T
ENST00000680000.1:c.3702+50A>T ENSP00000506173.1:n.3702+50A>T
ENST00000680135.1:c.*1666+50A>T ENSP00000506211.1:n.*1666+50A>T
ENST00000680149.1:c.3702+50A>T ENSP00000506497.1:n.3702+50A>T
ENST00000680163.1:c.3702+50A>T ENSP00000505092.1:n.3702+50A>T
ENST00000680174.1:n.4393+50A>T
ENST00000680236.1:c.*763+50A>T ENSP00000506212.1:n.*763+50A>T
ENST00000680497.1:c.3804+50A>T ENSP00000505954.1:n.3804+50A>T
ENST00000680508.1:c.3702+50A>T ENSP00000505749.1:n.3702+50A>T
ENST00000680569.1:c.*1413+50A>T ENSP00000505522.1:n.*1413+50A>T
ENST00000680630.1:n.4134+50A>T
ENST00000680634.1:n.21-2504A>T
ENST00000680722.1:n.1502+50A>T
ENST00000680723.1:n.4535A>T
ENST00000680726.1:c.3702+50A>T ENSP00000505505.1:n.3702+50A>T
ENST00000680737.1:n.3973+50A>T
ENST00000680759.1:c.3702+50A>T ENSP00000505848.1:n.3702+50A>T
ENST00000680814.1:c.3702+50A>T ENSP00000505710.1:n.3702+50A>T
ENST00000680828.1:c.*1274+50A>T ENSP00000505249.1:n.*1274+50A>T
ENST00000680861.1:c.3702+50A>T ENSP00000505043.1:n.3702+50A>T
ENST00000680927.1:c.3702+50A>T ENSP00000505473.1:n.3702+50A>T
ENST00000680939.1:n.4044+50A>T
ENST00000681152.1:c.*38A>T ENSP00000505388.1:n.*38A>T
ENST00000681250.1:c.*419+50A>T ENSP00000505684.1:n.*419+50A>T
ENST00000681256.1:c.*1720+50A>T ENSP00000505446.1:n.*1720+50A>T
ENST00000681279.1:n.4470+50A>T
ENST00000681303.1:c.*38A>T ENSP00000505576.1:n.*38A>T
ENST00000681307.1:n.4815+50A>T
ENST00000681461.1:n.4470+50A>T
ENST00000681495.1:c.1242+50A>T ENSP00000506085.1:n.1242+50A>T
ENST00000681558.1:c.1380+50A>T ENSP00000505568.1:n.1380+50A>T
ENST00000681619.1:c.3702+50A>T ENSP00000505071.1:n.3702+50A>T
ENST00000681716.1:c.*1413+50A>T ENSP00000505078.1:n.*1413+50A>T
ENST00000681758.1:n.4044+50A>T
ENST00000681768.1:c.*1366+50A>T ENSP00000506311.1:n.*1366+50A>T
ENST00000681808.1:c.3702+50A>T ENSP00000505219.1:n.3702+50A>T
ENST00000264276.10:c.3702+50A>T ENSP00000264276.6:n.3702+50A>T
ENST00000439495.5:c.1663+50A>T
ENST00000482891.5:n.3892A>T
ENST00000489440.5:n.523+50A>T
NM_020919.3:c.3702+50A>T NP_065970.2:n.3702+50A>T
XM_005246709.2:c.3702+50A>T XP_005246766.1:n.3702+50A>T
XM_006712654.1:c.3702+50A>T XP_006712717.1:n.3702+50A>T
XM_006712655.2:c.1638+50A>T XP_006712718.1:n.1638+50A>T
XM_011511530.1:c.3363+50A>T XP_011509832.1:n.3363+50A>T
XM_011511531.1:c.3702+50A>T XP_011509833.1:n.3702+50A>T
XR_922974.1:n.3837+50A>T
XM_006712654.3:c.3702+50A>T XP_006712717.1:n.3702+50A>T
XM_006712655.3:c.1638+50A>T XP_006712718.1:n.1638+50A>T
XM_017004569.2:c.3702+50A>T XP_016860058.1:n.3702+50A>T
XM_017004570.2:c.3702+50A>T XP_016860059.1:n.3702+50A>T
XM_017004572.2:c.1320+50A>T XP_016860061.1:n.1320+50A>T
XM_024453024.1:c.3363+50A>T XP_024308792.1:n.3363+50A>T
XM_024453025.1:c.1638+50A>T XP_024308793.1:n.1638+50A>T
XR_001738864.2:n.3837+50A>T
XR_001738865.2:n.3837+50A>T
XR_001738866.2:n.3837+50A>T
XR_001738867.2:n.3837+50A>T
XR_002959320.1:n.2893+50A>T
NM_020919.4:c.3702+50A>T MANE Select NP_065970.2:n.3702+50A>T