Canonical Allele Identifier: CA350319407

Gene: ALS2

Linked Data

• MyVariant Identifiers: chr2:g.202588126C>A (hg19) ; chr2:g.201723403C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201723403C>A , CM000664.2:g.201723403C>A	GRCh38
NC_000002.11:g.202588126C>A , CM000664.1:g.202588126C>A	GRCh37
NC_000002.10:g.202296371C>A	NCBI36
NG_008775.1:g.62770G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264276.11:c.3551G>T MANE Select	ENSP00000264276.6:p.Cys1184Phe
ENST00000439495.6:c.1229G>T	ENSP00000403832.2:p.Cys410Phe
ENST00000482891.6:n.4319G>T
ENST00000494017.6:n.1283G>T
ENST00000679409.1:c.1229G>T	ENSP00000506531.1:p.Cys410Phe
ENST00000679416.1:n.5055G>T
ENST00000679435.1:c.3551G>T	ENSP00000505218.1:p.Cys1184Phe
ENST00000679516.1:c.3551G>T	ENSP00000505187.1:p.Cys1184Phe
ENST00000679618.1:c.*639G>T	ENSP00000506274.1:n.*639G>T
ENST00000679630.1:n.5400G>T
ENST00000679686.1:n.3665G>T
ENST00000679701.1:n.6543G>T
ENST00000679916.1:c.3551G>T	ENSP00000506172.1:p.Cys1184Phe
ENST00000680000.1:c.3551G>T	ENSP00000506173.1:p.Cys1184Phe
ENST00000680135.1:c.*1515G>T	ENSP00000506211.1:n.*1515G>T
ENST00000680149.1:c.3551G>T	ENSP00000506497.1:p.Cys1184Phe
ENST00000680163.1:c.3551G>T	ENSP00000505092.1:p.Cys1184Phe
ENST00000680174.1:n.4242G>T
ENST00000680236.1:c.*612G>T	ENSP00000506212.1:n.*612G>T
ENST00000680497.1:c.3653G>T	ENSP00000505954.1:p.Cys1218Phe
ENST00000680508.1:c.3551G>T	ENSP00000505749.1:p.Cys1184Phe
ENST00000680569.1:c.*1262G>T	ENSP00000505522.1:n.*1262G>T
ENST00000680630.1:n.3983G>T
ENST00000680634.1:n.21-2914G>T
ENST00000680722.1:n.1351G>T
ENST00000680723.1:n.4334G>T
ENST00000680726.1:c.3551G>T	ENSP00000505505.1:p.Cys1184Phe
ENST00000680737.1:n.3822G>T
ENST00000680759.1:c.3551G>T	ENSP00000505848.1:p.Cys1184Phe
ENST00000680814.1:c.3551G>T	ENSP00000505710.1:p.Cys1184Phe
ENST00000680828.1:c.*1123G>T	ENSP00000505249.1:n.*1123G>T
ENST00000680861.1:c.3551G>T	ENSP00000505043.1:p.Cys1184Phe
ENST00000680927.1:c.3551G>T	ENSP00000505473.1:p.Cys1184Phe
ENST00000680939.1:n.3893G>T
ENST00000681152.1:c.3551G>T	ENSP00000505388.1:p.Cys1184Phe
ENST00000681250.1:c.*268G>T	ENSP00000505684.1:n.*268G>T
ENST00000681256.1:c.*1569G>T	ENSP00000505446.1:n.*1569G>T
ENST00000681279.1:n.4319G>T
ENST00000681303.1:c.3551G>T	ENSP00000505576.1:p.Cys1184Phe
ENST00000681307.1:n.4664G>T
ENST00000681461.1:n.4319G>T
ENST00000681495.1:c.1091G>T	ENSP00000506085.1:p.Cys364Phe
ENST00000681558.1:c.1229G>T	ENSP00000505568.1:p.Cys410Phe
ENST00000681619.1:c.3551G>T	ENSP00000505071.1:p.Cys1184Phe
ENST00000681716.1:c.*1262G>T	ENSP00000505078.1:n.*1262G>T
ENST00000681758.1:n.3893G>T
ENST00000681768.1:c.*1215G>T	ENSP00000506311.1:n.*1215G>T
ENST00000681808.1:c.3551G>T	ENSP00000505219.1:p.Cys1184Phe
ENST00000264276.10:c.3551G>T	ENSP00000264276.6:p.Cys1184Phe
ENST00000439495.5:c.1512G>T
ENST00000482891.5:n.3691G>T
ENST00000489440.5:n.372G>T
NM_020919.3:c.3551G>T	NP_065970.2:p.Cys1184Phe
XM_005246709.2:c.3551G>T	XP_005246766.1:p.Cys1184Phe
XM_006712654.1:c.3551G>T	XP_006712717.1:p.Cys1184Phe
XM_006712655.2:c.1487G>T	XP_006712718.1:p.Cys496Phe
XM_011511530.1:c.3212G>T	XP_011509832.1:p.Cys1071Phe
XM_011511531.1:c.3551G>T	XP_011509833.1:p.Cys1184Phe
XR_922974.1:n.3686G>T
XM_006712654.3:c.3551G>T	XP_006712717.1:p.Cys1184Phe
XM_006712655.3:c.1487G>T	XP_006712718.1:p.Cys496Phe
XM_017004569.2:c.3551G>T	XP_016860058.1:p.Cys1184Phe
XM_017004570.2:c.3551G>T	XP_016860059.1:p.Cys1184Phe
XM_017004572.2:c.1169G>T	XP_016860061.1:p.Cys390Phe
XM_024453024.1:c.3212G>T	XP_024308792.1:p.Cys1071Phe
XM_024453025.1:c.1487G>T	XP_024308793.1:p.Cys496Phe
XR_001738864.2:n.3686G>T
XR_001738865.2:n.3686G>T
XR_001738866.2:n.3686G>T
XR_001738867.2:n.3686G>T
XR_002959320.1:n.2742G>T
NM_020919.4:c.3551G>T MANE Select	NP_065970.2:p.Cys1184Phe