Canonical Allele Identifier: CA350324969

Gene: ALS2

Linked Data

• MyVariant Identifiers: chr2:g.202609020C>A (hg19) ; chr2:g.201744297C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201744297C>A , CM000664.2:g.201744297C>A	GRCh38
NC_000002.11:g.202609020C>A , CM000664.1:g.202609020C>A	GRCh37
NC_000002.10:g.202317265C>A	NCBI36
NG_008775.1:g.41876G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264276.11:c.2131G>T MANE Select	ENSP00000264276.6:p.Asp711Tyr
ENST00000482789.6:n.2473G>T
ENST00000482891.6:n.2473G>T
ENST00000679416.1:n.2473G>T
ENST00000679435.1:c.2131G>T	ENSP00000505218.1:p.Asp711Tyr
ENST00000679516.1:c.2131G>T	ENSP00000505187.1:p.Asp711Tyr
ENST00000679549.1:n.1360G>T
ENST00000679550.1:c.2131G>T	ENSP00000506193.1:p.Asp711Tyr
ENST00000679618.1:c.2131G>T	ENSP00000506274.1:p.Asp711Tyr
ENST00000679630.1:n.2473G>T
ENST00000679686.1:n.2245G>T
ENST00000679701.1:n.2473G>T
ENST00000679916.1:c.2131G>T	ENSP00000506172.1:p.Asp711Tyr
ENST00000679939.1:c.2131G>T	ENSP00000505704.1:p.Asp711Tyr
ENST00000679949.1:c.2083G>T	ENSP00000505232.1:p.Asp695Tyr
ENST00000680000.1:c.2131G>T	ENSP00000506173.1:p.Asp711Tyr
ENST00000680135.1:c.*95G>T	ENSP00000506211.1:n.*95G>T
ENST00000680149.1:c.2131G>T	ENSP00000506497.1:p.Asp711Tyr
ENST00000680163.1:c.2131G>T	ENSP00000505092.1:p.Asp711Tyr
ENST00000680174.1:n.2411G>T
ENST00000680236.1:c.2131G>T	ENSP00000506212.1:p.Asp711Tyr
ENST00000680287.1:c.2131G>T	ENSP00000506547.1:p.Asp711Tyr
ENST00000680497.1:c.2233G>T	ENSP00000505954.1:p.Asp745Tyr
ENST00000680508.1:c.2131G>T	ENSP00000505749.1:p.Asp711Tyr
ENST00000680569.1:c.2131G>T	ENSP00000505522.1:p.Asp711Tyr
ENST00000680630.1:n.2473G>T
ENST00000680644.1:c.*642G>T	ENSP00000505738.1:n.*642G>T
ENST00000680726.1:c.2131G>T	ENSP00000505505.1:p.Asp711Tyr
ENST00000680737.1:n.2473G>T
ENST00000680759.1:c.2131G>T	ENSP00000505848.1:p.Asp711Tyr
ENST00000680814.1:c.2131G>T	ENSP00000505710.1:p.Asp711Tyr
ENST00000680828.1:c.2131G>T	ENSP00000505249.1:p.Asp711Tyr
ENST00000680861.1:c.2131G>T	ENSP00000505043.1:p.Asp711Tyr
ENST00000680927.1:c.2131G>T	ENSP00000505473.1:p.Asp711Tyr
ENST00000680939.1:n.2473G>T
ENST00000681152.1:c.2131G>T	ENSP00000505388.1:p.Asp711Tyr
ENST00000681250.1:c.1471+13105G>T	ENSP00000505684.1:n.1471+13105G>T
ENST00000681256.1:c.1998+2269G>T	ENSP00000505446.1:n.1998+2269G>T
ENST00000681279.1:n.2473G>T
ENST00000681303.1:c.2131G>T	ENSP00000505576.1:p.Asp711Tyr
ENST00000681307.1:n.2473G>T
ENST00000681461.1:n.2473G>T
ENST00000681619.1:c.2131G>T	ENSP00000505071.1:p.Asp711Tyr
ENST00000681716.1:c.2131G>T	ENSP00000505078.1:p.Asp711Tyr
ENST00000681758.1:n.2473G>T
ENST00000681768.1:c.2131G>T	ENSP00000506311.1:p.Asp711Tyr
ENST00000681808.1:c.2131G>T	ENSP00000505219.1:p.Asp711Tyr
ENST00000264276.10:c.2131G>T	ENSP00000264276.6:p.Asp711Tyr
ENST00000439495.5:c.92G>T
ENST00000482789.5:n.2271G>T
ENST00000482891.5:n.2271G>T
NM_020919.3:c.2131G>T	NP_065970.2:p.Asp711Tyr
XM_005246709.2:c.2131G>T	XP_005246766.1:p.Asp711Tyr
XM_006712654.1:c.2131G>T	XP_006712717.1:p.Asp711Tyr
XM_006712655.2:c.67G>T	XP_006712718.1:p.Asp23Tyr
XM_011511530.1:c.1792G>T	XP_011509832.1:p.Asp598Tyr
XM_011511531.1:c.2131G>T	XP_011509833.1:p.Asp711Tyr
XR_922974.1:n.2266G>T
XM_006712654.3:c.2131G>T	XP_006712717.1:p.Asp711Tyr
XM_006712655.3:c.67G>T	XP_006712718.1:p.Asp23Tyr
XM_017004569.2:c.2131G>T	XP_016860058.1:p.Asp711Tyr
XM_017004570.2:c.2131G>T	XP_016860059.1:p.Asp711Tyr
XM_017004572.2:c.-355G>T	XP_016860061.1:n.-355G>T
XM_024453024.1:c.1792G>T	XP_024308792.1:p.Asp598Tyr
XM_024453025.1:c.67G>T	XP_024308793.1:p.Asp23Tyr
XR_001738864.2:n.2266G>T
XR_001738865.2:n.2266G>T
XR_001738866.2:n.2266G>T
XR_001738867.2:n.2266G>T
XR_002959320.1:n.1322G>T
NM_020919.4:c.2131G>T MANE Select	NP_065970.2:p.Asp711Tyr