Canonical Allele Identifier: CA1321178645
Gene: ALS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201724415A= , CM000664.2:g.201724415A= GRCh38
NC_000002.11:g.202589138A= , CM000664.1:g.202589138A= GRCh37
NC_000002.10:g.202297383A= NCBI36
NG_008775.1:g.61758T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264276.11:c.3392T= MANE Select ENSP00000264276.6:p.Met1131=
ENST00000439495.6:c.1070T= ENSP00000403832.2:p.Met357=
ENST00000482891.6:n.4160T=
ENST00000494017.6:n.1124T=
ENST00000679409.1:c.1070T= ENSP00000506531.1:p.Met357=
ENST00000679416.1:n.4896T=
ENST00000679435.1:c.3392T= ENSP00000505218.1:p.Met1131=
ENST00000679516.1:c.3392T= ENSP00000505187.1:p.Met1131=
ENST00000679618.1:c.*480T= ENSP00000506274.1:n.*480T=
ENST00000679630.1:n.5241T=
ENST00000679686.1:n.3506T=
ENST00000679701.1:n.6384T=
ENST00000679916.1:c.3392T= ENSP00000506172.1:p.Met1131=
ENST00000680000.1:c.3392T= ENSP00000506173.1:p.Met1131=
ENST00000680135.1:c.*1356T= ENSP00000506211.1:n.*1356T=
ENST00000680149.1:c.3392T= ENSP00000506497.1:p.Met1131=
ENST00000680163.1:c.3392T= ENSP00000505092.1:p.Met1131=
ENST00000680174.1:n.4083T=
ENST00000680236.1:c.*453T= ENSP00000506212.1:n.*453T=
ENST00000680497.1:c.3494T= ENSP00000505954.1:p.Met1165=
ENST00000680508.1:c.3392T= ENSP00000505749.1:p.Met1131=
ENST00000680569.1:c.*1103T= ENSP00000505522.1:n.*1103T=
ENST00000680630.1:n.3824T=
ENST00000680634.1:n.21-3926T=
ENST00000680722.1:n.1192T=
ENST00000680723.1:n.4175T=
ENST00000680726.1:c.3392T= ENSP00000505505.1:p.Met1131=
ENST00000680737.1:n.3663T=
ENST00000680759.1:c.3392T= ENSP00000505848.1:p.Met1131=
ENST00000680814.1:c.3392T= ENSP00000505710.1:p.Met1131=
ENST00000680828.1:c.*964T= ENSP00000505249.1:n.*964T=
ENST00000680861.1:c.3392T= ENSP00000505043.1:p.Met1131=
ENST00000680927.1:c.3392T= ENSP00000505473.1:p.Met1131=
ENST00000680939.1:n.3734T=
ENST00000681152.1:c.3392T= ENSP00000505388.1:p.Met1131=
ENST00000681250.1:c.*109T= ENSP00000505684.1:n.*109T=
ENST00000681256.1:c.*1410T= ENSP00000505446.1:n.*1410T=
ENST00000681279.1:n.4160T=
ENST00000681303.1:c.3392T= ENSP00000505576.1:p.Met1131=
ENST00000681307.1:n.4505T=
ENST00000681461.1:n.4160T=
ENST00000681495.1:c.932T= ENSP00000506085.1:p.Met311=
ENST00000681558.1:c.1070T= ENSP00000505568.1:p.Met357=
ENST00000681619.1:c.3392T= ENSP00000505071.1:p.Met1131=
ENST00000681716.1:c.*1103T= ENSP00000505078.1:n.*1103T=
ENST00000681758.1:n.3734T=
ENST00000681768.1:c.*1056T= ENSP00000506311.1:n.*1056T=
ENST00000681808.1:c.3392T= ENSP00000505219.1:p.Met1131=
ENST00000264276.10:c.3392T= ENSP00000264276.6:p.Met1131=
ENST00000439495.5:c.1353T=
ENST00000482891.5:n.3532T=
ENST00000489440.5:n.213T=
NM_020919.3:c.3392T= NP_065970.2:p.Met1131=
XM_005246709.2:c.3392T= XP_005246766.1:p.Met1131=
XM_006712654.1:c.3392T= XP_006712717.1:p.Met1131=
XM_006712655.2:c.1328T= XP_006712718.1:p.Met443=
XM_011511530.1:c.3053T= XP_011509832.1:p.Met1018=
XM_011511531.1:c.3392T= XP_011509833.1:p.Met1131=
XR_922974.1:n.3527T=
XM_006712654.3:c.3392T= XP_006712717.1:p.Met1131=
XM_006712655.3:c.1328T= XP_006712718.1:p.Met443=
XM_017004569.2:c.3392T= XP_016860058.1:p.Met1131=
XM_017004570.2:c.3392T= XP_016860059.1:p.Met1131=
XM_017004572.2:c.1010T= XP_016860061.1:p.Met337=
XM_024453024.1:c.3053T= XP_024308792.1:p.Met1018=
XM_024453025.1:c.1328T= XP_024308793.1:p.Met443=
XR_001738864.2:n.3527T=
XR_001738865.2:n.3527T=
XR_001738866.2:n.3527T=
XR_001738867.2:n.3527T=
XR_002959320.1:n.2583T=
NM_020919.4:c.3392T= MANE Select NP_065970.2:p.Met1131=