Canonical Allele Identifier: CA1321156483
Gene: ALS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201704095A= , CM000664.2:g.201704095A= GRCh38
NC_000002.11:g.202568818A= , CM000664.1:g.202568818A= GRCh37
NC_000002.10:g.202277063A= NCBI36
NG_008775.1:g.82078T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264276.11:c.4935+27T= MANE Select ENSP00000264276.6:n.4935+27T=
ENST00000439495.6:c.*1115+27T= ENSP00000403832.2:n.*1115+27T=
ENST00000679409.1:c.*1667T= ENSP00000506531.1:n.*1667T=
ENST00000679416.1:n.6439+27T=
ENST00000679427.1:n.2633T=
ENST00000679435.1:c.4935+27T= ENSP00000505218.1:n.4935+27T=
ENST00000679516.1:c.4935+27T= ENSP00000505187.1:n.4935+27T=
ENST00000679618.1:c.*2023+27T= ENSP00000506274.1:n.*2023+27T=
ENST00000679630.1:n.6784+27T=
ENST00000679635.1:n.3197+27T=
ENST00000679686.1:n.5049+27T=
ENST00000679701.1:n.7927+27T=
ENST00000679916.1:c.*1283+27T= ENSP00000506172.1:n.*1283+27T=
ENST00000680000.1:c.*6T= ENSP00000506173.1:n.*6T=
ENST00000680135.1:c.*2896+27T= ENSP00000506211.1:n.*2896+27T=
ENST00000680149.1:c.*217+27T= ENSP00000506497.1:n.*217+27T=
ENST00000680163.1:c.4935+27T= ENSP00000505092.1:n.4935+27T=
ENST00000680174.1:n.5626+27T=
ENST00000680236.1:c.*1996+27T= ENSP00000506212.1:n.*1996+27T=
ENST00000680404.1:n.477T=
ENST00000680441.1:n.3493+27T=
ENST00000680497.1:c.5037+27T= ENSP00000505954.1:n.5037+27T=
ENST00000680508.1:c.*91+27T= ENSP00000505749.1:n.*91+27T=
ENST00000680569.1:c.*2878+27T= ENSP00000505522.1:n.*2878+27T=
ENST00000680634.1:n.1443+27T=
ENST00000680722.1:n.2735+27T=
ENST00000680726.1:c.*217+27T= ENSP00000505505.1:n.*217+27T=
ENST00000680759.1:c.4767+27T= ENSP00000505848.1:n.4767+27T=
ENST00000680814.1:c.4838+359T= ENSP00000505710.1:n.4838+359T=
ENST00000680828.1:c.*2629+27T= ENSP00000505249.1:n.*2629+27T=
ENST00000680861.1:c.4935+27T= ENSP00000505043.1:n.4935+27T=
ENST00000680927.1:c.*1115+27T= ENSP00000505473.1:n.*1115+27T=
ENST00000680939.1:n.6903T=
ENST00000681250.1:c.*1652+27T= ENSP00000505684.1:n.*1652+27T=
ENST00000681256.1:c.*2950+27T= ENSP00000505446.1:n.*2950+27T=
ENST00000681279.1:n.5801+27T=
ENST00000681307.1:n.6048+27T=
ENST00000681461.1:n.5703+27T=
ENST00000681495.1:c.2472+27T= ENSP00000506085.1:n.2472+27T=
ENST00000681558.1:c.2613+27T= ENSP00000505568.1:n.2613+27T=
ENST00000681619.1:c.4932+27T= ENSP00000505071.1:n.4932+27T=
ENST00000681663.1:n.1841+27T=
ENST00000681692.1:n.2895+27T=
ENST00000681716.1:c.*2789+27T= ENSP00000505078.1:n.*2789+27T=
ENST00000681768.1:c.*2599+27T= ENSP00000506311.1:n.*2599+27T=
ENST00000681808.1:c.4758+27T= ENSP00000505219.1:n.4758+27T=
ENST00000264276.10:c.4935+27T= ENSP00000264276.6:n.4935+27T=
ENST00000439495.5:c.3039+27T=
NM_020919.3:c.4935+27T= NP_065970.2:n.4935+27T=
XM_005246709.2:c.4932+27T= XP_005246766.1:n.4932+27T=
XM_006712654.1:c.4935+27T= XP_006712717.1:n.4935+27T=
XM_006712655.2:c.2871+27T= XP_006712718.1:n.2871+27T=
XM_011511530.1:c.4596+27T= XP_011509832.1:n.4596+27T=
XR_922974.1:n.5213+27T=
XM_006712654.3:c.4935+27T= XP_006712717.1:n.4935+27T=
XM_006712655.3:c.2871+27T= XP_006712718.1:n.2871+27T=
XM_017004569.2:c.4932+27T= XP_016860058.1:n.4932+27T=
XM_017004572.2:c.2553+27T= XP_016860061.1:n.2553+27T=
XM_024453024.1:c.4596+27T= XP_024308792.1:n.4596+27T=
XM_024453025.1:c.2868+27T= XP_024308793.1:n.2868+27T=
XR_001738864.2:n.5050+27T=
XR_001738865.2:n.5047+27T=
XR_001738866.2:n.5213+27T=
XR_001738867.2:n.5210+27T=
XR_002959320.1:n.4106+27T=
NM_020919.4:c.4935+27T= MANE Select NP_065970.2:n.4935+27T=