Canonical Allele Identifier: CA2057955

Gene: ALS2

Linked Data

• ClinVar Variation Id: 333592
• ClinVar RCV Id: RCV000261194 ; RCV000355910 ; RCV000515815 ; RCV000863616 ; RCV001260560 ; RCV001590976
• dbSNP Id: rs200706696
• ExAC: 2:202591249 C / T
• gnomAD v2: 2-202591249-C-T
• gnomAD v3: 2-201726526-C-T
• gnomAD v4: 2-201726526-C-T
• COSMIC: COSM3695197
• MyVariant Identifiers: chr2:g.202591249C>T (hg19) ; chr2:g.201726526C>T (hg38)
• PubMed: PMID:28832565

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201726526C>T , CM000664.2:g.201726526C>T	GRCh38
NC_000002.11:g.202591249C>T , CM000664.1:g.202591249C>T	GRCh37
NC_000002.10:g.202299494C>T	NCBI36
NG_008775.1:g.59647G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264276.11:c.3206G>A MANE Select	ENSP00000264276.6:p.Gly1069Glu
ENST00000439495.6:c.884G>A	ENSP00000403832.2:p.Gly295Glu
ENST00000482891.6:n.3974G>A
ENST00000494017.6:n.938G>A
ENST00000679409.1:c.884G>A	ENSP00000506531.1:p.Gly295Glu
ENST00000679416.1:n.4710G>A
ENST00000679435.1:c.3206G>A	ENSP00000505218.1:p.Gly1069Glu
ENST00000679516.1:c.3206G>A	ENSP00000505187.1:p.Gly1069Glu
ENST00000679618.1:c.*294G>A	ENSP00000506274.1:n.*294G>A
ENST00000679630.1:n.5055G>A
ENST00000679686.1:n.3320G>A
ENST00000679701.1:n.5169G>A
ENST00000679916.1:c.3206G>A	ENSP00000506172.1:p.Gly1069Glu
ENST00000680000.1:c.3206G>A	ENSP00000506173.1:p.Gly1069Glu
ENST00000680135.1:c.*1170G>A	ENSP00000506211.1:n.*1170G>A
ENST00000680149.1:c.3206G>A	ENSP00000506497.1:p.Gly1069Glu
ENST00000680163.1:c.3206G>A	ENSP00000505092.1:p.Gly1069Glu
ENST00000680174.1:n.3897G>A
ENST00000680236.1:c.*267G>A	ENSP00000506212.1:n.*267G>A
ENST00000680497.1:c.3308G>A	ENSP00000505954.1:p.Gly1103Glu
ENST00000680508.1:c.3206G>A	ENSP00000505749.1:p.Gly1069Glu
ENST00000680569.1:c.*917G>A	ENSP00000505522.1:n.*917G>A
ENST00000680630.1:n.3638G>A
ENST00000680634.1:n.21-6037G>A
ENST00000680722.1:n.1006G>A
ENST00000680723.1:n.2960G>A
ENST00000680726.1:c.3206G>A	ENSP00000505505.1:p.Gly1069Glu
ENST00000680737.1:n.3477G>A
ENST00000680759.1:c.3206G>A	ENSP00000505848.1:p.Gly1069Glu
ENST00000680814.1:c.3206G>A	ENSP00000505710.1:p.Gly1069Glu
ENST00000680828.1:c.*778G>A	ENSP00000505249.1:n.*778G>A
ENST00000680861.1:c.3206G>A	ENSP00000505043.1:p.Gly1069Glu
ENST00000680927.1:c.3206G>A	ENSP00000505473.1:p.Gly1069Glu
ENST00000680939.1:n.3548G>A
ENST00000681152.1:c.3206G>A	ENSP00000505388.1:p.Gly1069Glu
ENST00000681250.1:c.1472-1072G>A	ENSP00000505684.1:n.1472-1072G>A
ENST00000681256.1:c.*1224G>A	ENSP00000505446.1:n.*1224G>A
ENST00000681279.1:n.3974G>A
ENST00000681303.1:c.3206G>A	ENSP00000505576.1:p.Gly1069Glu
ENST00000681307.1:n.4319G>A
ENST00000681461.1:n.3974G>A
ENST00000681495.1:c.746G>A	ENSP00000506085.1:p.Gly249Glu
ENST00000681558.1:c.884G>A	ENSP00000505568.1:p.Gly295Glu
ENST00000681619.1:c.3206G>A	ENSP00000505071.1:p.Gly1069Glu
ENST00000681716.1:c.*917G>A	ENSP00000505078.1:n.*917G>A
ENST00000681758.1:n.3548G>A
ENST00000681768.1:c.*870G>A	ENSP00000506311.1:n.*870G>A
ENST00000681808.1:c.3206G>A	ENSP00000505219.1:p.Gly1069Glu
ENST00000264276.10:c.3206G>A	ENSP00000264276.6:p.Gly1069Glu
ENST00000439495.5:c.1167G>A
ENST00000482891.5:n.3346G>A
ENST00000489440.5:n.27G>A
NM_020919.3:c.3206G>A	NP_065970.2:p.Gly1069Glu
XM_005246709.2:c.3206G>A	XP_005246766.1:p.Gly1069Glu
XM_006712654.1:c.3206G>A	XP_006712717.1:p.Gly1069Glu
XM_006712655.2:c.1142G>A	XP_006712718.1:p.Gly381Glu
XM_011511530.1:c.2867G>A	XP_011509832.1:p.Gly956Glu
XM_011511531.1:c.3206G>A	XP_011509833.1:p.Gly1069Glu
XR_922974.1:n.3341G>A
XM_006712654.3:c.3206G>A	XP_006712717.1:p.Gly1069Glu
XM_006712655.3:c.1142G>A	XP_006712718.1:p.Gly381Glu
XM_017004569.2:c.3206G>A	XP_016860058.1:p.Gly1069Glu
XM_017004570.2:c.3206G>A	XP_016860059.1:p.Gly1069Glu
XM_017004572.2:c.824G>A	XP_016860061.1:p.Gly275Glu
XM_024453024.1:c.2867G>A	XP_024308792.1:p.Gly956Glu
XM_024453025.1:c.1142G>A	XP_024308793.1:p.Gly381Glu
XR_001738864.2:n.3341G>A
XR_001738865.2:n.3341G>A
XR_001738866.2:n.3341G>A
XR_001738867.2:n.3341G>A
XR_002959320.1:n.2397G>A
NM_020919.4:c.3206G>A MANE Select	NP_065970.2:p.Gly1069Glu