Canonical Allele Identifier: CA350319866

Gene: ALS2

Linked Data

• MyVariant Identifiers: chr2:g.202589156C>G (hg19) ; chr2:g.201724433C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201724433C>G , CM000664.2:g.201724433C>G	GRCh38
NC_000002.11:g.202589156C>G , CM000664.1:g.202589156C>G	GRCh37
NC_000002.10:g.202297401C>G	NCBI36
NG_008775.1:g.61740G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264276.11:c.3374G>C MANE Select	ENSP00000264276.6:p.Gly1125Ala
ENST00000439495.6:c.1052G>C	ENSP00000403832.2:p.Gly351Ala
ENST00000482891.6:n.4142G>C
ENST00000494017.6:n.1106G>C
ENST00000679409.1:c.1052G>C	ENSP00000506531.1:p.Gly351Ala
ENST00000679416.1:n.4878G>C
ENST00000679435.1:c.3374G>C	ENSP00000505218.1:p.Gly1125Ala
ENST00000679516.1:c.3374G>C	ENSP00000505187.1:p.Gly1125Ala
ENST00000679618.1:c.*462G>C	ENSP00000506274.1:n.*462G>C
ENST00000679630.1:n.5223G>C
ENST00000679686.1:n.3488G>C
ENST00000679701.1:n.6366G>C
ENST00000679916.1:c.3374G>C	ENSP00000506172.1:p.Gly1125Ala
ENST00000680000.1:c.3374G>C	ENSP00000506173.1:p.Gly1125Ala
ENST00000680135.1:c.*1338G>C	ENSP00000506211.1:n.*1338G>C
ENST00000680149.1:c.3374G>C	ENSP00000506497.1:p.Gly1125Ala
ENST00000680163.1:c.3374G>C	ENSP00000505092.1:p.Gly1125Ala
ENST00000680174.1:n.4065G>C
ENST00000680236.1:c.*435G>C	ENSP00000506212.1:n.*435G>C
ENST00000680497.1:c.3476G>C	ENSP00000505954.1:p.Gly1159Ala
ENST00000680508.1:c.3374G>C	ENSP00000505749.1:p.Gly1125Ala
ENST00000680569.1:c.*1085G>C	ENSP00000505522.1:n.*1085G>C
ENST00000680630.1:n.3806G>C
ENST00000680634.1:n.21-3944G>C
ENST00000680722.1:n.1174G>C
ENST00000680723.1:n.4157G>C
ENST00000680726.1:c.3374G>C	ENSP00000505505.1:p.Gly1125Ala
ENST00000680737.1:n.3645G>C
ENST00000680759.1:c.3374G>C	ENSP00000505848.1:p.Gly1125Ala
ENST00000680814.1:c.3374G>C	ENSP00000505710.1:p.Gly1125Ala
ENST00000680828.1:c.*946G>C	ENSP00000505249.1:n.*946G>C
ENST00000680861.1:c.3374G>C	ENSP00000505043.1:p.Gly1125Ala
ENST00000680927.1:c.3374G>C	ENSP00000505473.1:p.Gly1125Ala
ENST00000680939.1:n.3716G>C
ENST00000681152.1:c.3374G>C	ENSP00000505388.1:p.Gly1125Ala
ENST00000681250.1:c.*91G>C	ENSP00000505684.1:n.*91G>C
ENST00000681256.1:c.*1392G>C	ENSP00000505446.1:n.*1392G>C
ENST00000681279.1:n.4142G>C
ENST00000681303.1:c.3374G>C	ENSP00000505576.1:p.Gly1125Ala
ENST00000681307.1:n.4487G>C
ENST00000681461.1:n.4142G>C
ENST00000681495.1:c.914G>C	ENSP00000506085.1:p.Gly305Ala
ENST00000681558.1:c.1052G>C	ENSP00000505568.1:p.Gly351Ala
ENST00000681619.1:c.3374G>C	ENSP00000505071.1:p.Gly1125Ala
ENST00000681716.1:c.*1085G>C	ENSP00000505078.1:n.*1085G>C
ENST00000681758.1:n.3716G>C
ENST00000681768.1:c.*1038G>C	ENSP00000506311.1:n.*1038G>C
ENST00000681808.1:c.3374G>C	ENSP00000505219.1:p.Gly1125Ala
ENST00000264276.10:c.3374G>C	ENSP00000264276.6:p.Gly1125Ala
ENST00000439495.5:c.1335G>C
ENST00000482891.5:n.3514G>C
ENST00000489440.5:n.195G>C
NM_020919.3:c.3374G>C	NP_065970.2:p.Gly1125Ala
XM_005246709.2:c.3374G>C	XP_005246766.1:p.Gly1125Ala
XM_006712654.1:c.3374G>C	XP_006712717.1:p.Gly1125Ala
XM_006712655.2:c.1310G>C	XP_006712718.1:p.Gly437Ala
XM_011511530.1:c.3035G>C	XP_011509832.1:p.Gly1012Ala
XM_011511531.1:c.3374G>C	XP_011509833.1:p.Gly1125Ala
XR_922974.1:n.3509G>C
XM_006712654.3:c.3374G>C	XP_006712717.1:p.Gly1125Ala
XM_006712655.3:c.1310G>C	XP_006712718.1:p.Gly437Ala
XM_017004569.2:c.3374G>C	XP_016860058.1:p.Gly1125Ala
XM_017004570.2:c.3374G>C	XP_016860059.1:p.Gly1125Ala
XM_017004572.2:c.992G>C	XP_016860061.1:p.Gly331Ala
XM_024453024.1:c.3035G>C	XP_024308792.1:p.Gly1012Ala
XM_024453025.1:c.1310G>C	XP_024308793.1:p.Gly437Ala
XR_001738864.2:n.3509G>C
XR_001738865.2:n.3509G>C
XR_001738866.2:n.3509G>C
XR_001738867.2:n.3509G>C
XR_002959320.1:n.2565G>C
NM_020919.4:c.3374G>C MANE Select	NP_065970.2:p.Gly1125Ala