Canonical Allele Identifier: CA350319551

Gene: ALS2

Linked Data

• gnomAD v4: 2-201723441-C-A
• MyVariant Identifiers: chr2:g.202588164C>A (hg19) ; chr2:g.201723441C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201723441C>A , CM000664.2:g.201723441C>A	GRCh38
NC_000002.11:g.202588164C>A , CM000664.1:g.202588164C>A	GRCh37
NC_000002.10:g.202296409C>A	NCBI36
NG_008775.1:g.62732G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264276.11:c.3513G>T MANE Select	ENSP00000264276.6:p.Arg1171Ser
ENST00000439495.6:c.1191G>T	ENSP00000403832.2:p.Arg397Ser
ENST00000482891.6:n.4281G>T
ENST00000494017.6:n.1245G>T
ENST00000679409.1:c.1191G>T	ENSP00000506531.1:p.Arg397Ser
ENST00000679416.1:n.5017G>T
ENST00000679435.1:c.3513G>T	ENSP00000505218.1:p.Arg1171Ser
ENST00000679516.1:c.3513G>T	ENSP00000505187.1:p.Arg1171Ser
ENST00000679618.1:c.*601G>T	ENSP00000506274.1:n.*601G>T
ENST00000679630.1:n.5362G>T
ENST00000679686.1:n.3627G>T
ENST00000679701.1:n.6505G>T
ENST00000679916.1:c.3513G>T	ENSP00000506172.1:p.Arg1171Ser
ENST00000680000.1:c.3513G>T	ENSP00000506173.1:p.Arg1171Ser
ENST00000680135.1:c.*1477G>T	ENSP00000506211.1:n.*1477G>T
ENST00000680149.1:c.3513G>T	ENSP00000506497.1:p.Arg1171Ser
ENST00000680163.1:c.3513G>T	ENSP00000505092.1:p.Arg1171Ser
ENST00000680174.1:n.4204G>T
ENST00000680236.1:c.*574G>T	ENSP00000506212.1:n.*574G>T
ENST00000680497.1:c.3615G>T	ENSP00000505954.1:p.Arg1205Ser
ENST00000680508.1:c.3513G>T	ENSP00000505749.1:p.Arg1171Ser
ENST00000680569.1:c.*1224G>T	ENSP00000505522.1:n.*1224G>T
ENST00000680630.1:n.3945G>T
ENST00000680634.1:n.21-2952G>T
ENST00000680722.1:n.1313G>T
ENST00000680723.1:n.4296G>T
ENST00000680726.1:c.3513G>T	ENSP00000505505.1:p.Arg1171Ser
ENST00000680737.1:n.3784G>T
ENST00000680759.1:c.3513G>T	ENSP00000505848.1:p.Arg1171Ser
ENST00000680814.1:c.3513G>T	ENSP00000505710.1:p.Arg1171Ser
ENST00000680828.1:c.*1085G>T	ENSP00000505249.1:n.*1085G>T
ENST00000680861.1:c.3513G>T	ENSP00000505043.1:p.Arg1171Ser
ENST00000680927.1:c.3513G>T	ENSP00000505473.1:p.Arg1171Ser
ENST00000680939.1:n.3855G>T
ENST00000681152.1:c.3513G>T	ENSP00000505388.1:p.Arg1171Ser
ENST00000681250.1:c.*230G>T	ENSP00000505684.1:n.*230G>T
ENST00000681256.1:c.*1531G>T	ENSP00000505446.1:n.*1531G>T
ENST00000681279.1:n.4281G>T
ENST00000681303.1:c.3513G>T	ENSP00000505576.1:p.Arg1171Ser
ENST00000681307.1:n.4626G>T
ENST00000681461.1:n.4281G>T
ENST00000681495.1:c.1053G>T	ENSP00000506085.1:p.Arg351Ser
ENST00000681558.1:c.1191G>T	ENSP00000505568.1:p.Arg397Ser
ENST00000681619.1:c.3513G>T	ENSP00000505071.1:p.Arg1171Ser
ENST00000681716.1:c.*1224G>T	ENSP00000505078.1:n.*1224G>T
ENST00000681758.1:n.3855G>T
ENST00000681768.1:c.*1177G>T	ENSP00000506311.1:n.*1177G>T
ENST00000681808.1:c.3513G>T	ENSP00000505219.1:p.Arg1171Ser
ENST00000264276.10:c.3513G>T	ENSP00000264276.6:p.Arg1171Ser
ENST00000439495.5:c.1474G>T
ENST00000482891.5:n.3653G>T
ENST00000489440.5:n.334G>T
NM_020919.3:c.3513G>T	NP_065970.2:p.Arg1171Ser
XM_005246709.2:c.3513G>T	XP_005246766.1:p.Arg1171Ser
XM_006712654.1:c.3513G>T	XP_006712717.1:p.Arg1171Ser
XM_006712655.2:c.1449G>T	XP_006712718.1:p.Arg483Ser
XM_011511530.1:c.3174G>T	XP_011509832.1:p.Arg1058Ser
XM_011511531.1:c.3513G>T	XP_011509833.1:p.Arg1171Ser
XR_922974.1:n.3648G>T
XM_006712654.3:c.3513G>T	XP_006712717.1:p.Arg1171Ser
XM_006712655.3:c.1449G>T	XP_006712718.1:p.Arg483Ser
XM_017004569.2:c.3513G>T	XP_016860058.1:p.Arg1171Ser
XM_017004570.2:c.3513G>T	XP_016860059.1:p.Arg1171Ser
XM_017004572.2:c.1131G>T	XP_016860061.1:p.Arg377Ser
XM_024453024.1:c.3174G>T	XP_024308792.1:p.Arg1058Ser
XM_024453025.1:c.1449G>T	XP_024308793.1:p.Arg483Ser
XR_001738864.2:n.3648G>T
XR_001738865.2:n.3648G>T
XR_001738866.2:n.3648G>T
XR_001738867.2:n.3648G>T
XR_002959320.1:n.2704G>T
NM_020919.4:c.3513G>T MANE Select	NP_065970.2:p.Arg1171Ser