Canonical Allele Identifier: CA350319877
Gene: ALS2 HGNC NCBI

Linked Data

dbSNP Id: rs1226366041

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201724437C>T , CM000664.2:g.201724437C>T GRCh38
NC_000002.11:g.202589160C>T , CM000664.1:g.202589160C>T GRCh37
NC_000002.10:g.202297405C>T NCBI36
NG_008775.1:g.61736G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264276.11:c.3370G>A MANE Select ENSP00000264276.6:p.Glu1124Lys
ENST00000439495.6:c.1048G>A ENSP00000403832.2:p.Glu350Lys
ENST00000482891.6:n.4138G>A
ENST00000494017.6:n.1102G>A
ENST00000679409.1:c.1048G>A ENSP00000506531.1:p.Glu350Lys
ENST00000679416.1:n.4874G>A
ENST00000679435.1:c.3370G>A ENSP00000505218.1:p.Glu1124Lys
ENST00000679516.1:c.3370G>A ENSP00000505187.1:p.Glu1124Lys
ENST00000679618.1:c.*458G>A ENSP00000506274.1:n.*458G>A
ENST00000679630.1:n.5219G>A
ENST00000679686.1:n.3484G>A
ENST00000679701.1:n.6362G>A
ENST00000679916.1:c.3370G>A ENSP00000506172.1:p.Glu1124Lys
ENST00000680000.1:c.3370G>A ENSP00000506173.1:p.Glu1124Lys
ENST00000680135.1:c.*1334G>A ENSP00000506211.1:n.*1334G>A
ENST00000680149.1:c.3370G>A ENSP00000506497.1:p.Glu1124Lys
ENST00000680163.1:c.3370G>A ENSP00000505092.1:p.Glu1124Lys
ENST00000680174.1:n.4061G>A
ENST00000680236.1:c.*431G>A ENSP00000506212.1:n.*431G>A
ENST00000680497.1:c.3472G>A ENSP00000505954.1:p.Glu1158Lys
ENST00000680508.1:c.3370G>A ENSP00000505749.1:p.Glu1124Lys
ENST00000680569.1:c.*1081G>A ENSP00000505522.1:n.*1081G>A
ENST00000680630.1:n.3802G>A
ENST00000680634.1:n.21-3948G>A
ENST00000680722.1:n.1170G>A
ENST00000680723.1:n.4153G>A
ENST00000680726.1:c.3370G>A ENSP00000505505.1:p.Glu1124Lys
ENST00000680737.1:n.3641G>A
ENST00000680759.1:c.3370G>A ENSP00000505848.1:p.Glu1124Lys
ENST00000680814.1:c.3370G>A ENSP00000505710.1:p.Glu1124Lys
ENST00000680828.1:c.*942G>A ENSP00000505249.1:n.*942G>A
ENST00000680861.1:c.3370G>A ENSP00000505043.1:p.Glu1124Lys
ENST00000680927.1:c.3370G>A ENSP00000505473.1:p.Glu1124Lys
ENST00000680939.1:n.3712G>A
ENST00000681152.1:c.3370G>A ENSP00000505388.1:p.Glu1124Lys
ENST00000681250.1:c.*87G>A ENSP00000505684.1:n.*87G>A
ENST00000681256.1:c.*1388G>A ENSP00000505446.1:n.*1388G>A
ENST00000681279.1:n.4138G>A
ENST00000681303.1:c.3370G>A ENSP00000505576.1:p.Glu1124Lys
ENST00000681307.1:n.4483G>A
ENST00000681461.1:n.4138G>A
ENST00000681495.1:c.910G>A ENSP00000506085.1:p.Glu304Lys
ENST00000681558.1:c.1048G>A ENSP00000505568.1:p.Glu350Lys
ENST00000681619.1:c.3370G>A ENSP00000505071.1:p.Glu1124Lys
ENST00000681716.1:c.*1081G>A ENSP00000505078.1:n.*1081G>A
ENST00000681758.1:n.3712G>A
ENST00000681768.1:c.*1034G>A ENSP00000506311.1:n.*1034G>A
ENST00000681808.1:c.3370G>A ENSP00000505219.1:p.Glu1124Lys
ENST00000264276.10:c.3370G>A ENSP00000264276.6:p.Glu1124Lys
ENST00000439495.5:c.1331G>A
ENST00000482891.5:n.3510G>A
ENST00000489440.5:n.191G>A
NM_020919.3:c.3370G>A NP_065970.2:p.Glu1124Lys
XM_005246709.2:c.3370G>A XP_005246766.1:p.Glu1124Lys
XM_006712654.1:c.3370G>A XP_006712717.1:p.Glu1124Lys
XM_006712655.2:c.1306G>A XP_006712718.1:p.Glu436Lys
XM_011511530.1:c.3031G>A XP_011509832.1:p.Glu1011Lys
XM_011511531.1:c.3370G>A XP_011509833.1:p.Glu1124Lys
XR_922974.1:n.3505G>A
XM_006712654.3:c.3370G>A XP_006712717.1:p.Glu1124Lys
XM_006712655.3:c.1306G>A XP_006712718.1:p.Glu436Lys
XM_017004569.2:c.3370G>A XP_016860058.1:p.Glu1124Lys
XM_017004570.2:c.3370G>A XP_016860059.1:p.Glu1124Lys
XM_017004572.2:c.988G>A XP_016860061.1:p.Glu330Lys
XM_024453024.1:c.3031G>A XP_024308792.1:p.Glu1011Lys
XM_024453025.1:c.1306G>A XP_024308793.1:p.Glu436Lys
XR_001738864.2:n.3505G>A
XR_001738865.2:n.3505G>A
XR_001738866.2:n.3505G>A
XR_001738867.2:n.3505G>A
XR_002959320.1:n.2561G>A
NM_020919.4:c.3370G>A MANE Select NP_065970.2:p.Glu1124Lys