Canonical Allele Identifier: CA2057828

Gene: ALS2

Linked Data

• dbSNP Id: rs764616850
• ExAC: 2:202588064 T / C
• gnomAD v2: 2-202588064-T-C
• MyVariant Identifiers: chr2:g.202588064T>C (hg19) ; chr2:g.201723341T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201723341T>C , CM000664.2:g.201723341T>C	GRCh38
NC_000002.11:g.202588064T>C , CM000664.1:g.202588064T>C	GRCh37
NC_000002.10:g.202296309T>C	NCBI36
NG_008775.1:g.62832A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264276.11:c.3613A>G MANE Select	ENSP00000264276.6:p.Asn1205Asp
ENST00000439495.6:c.1291A>G	ENSP00000403832.2:p.Asn431Asp
ENST00000482891.6:n.4381A>G
ENST00000494017.6:n.1345A>G
ENST00000679409.1:c.1291A>G	ENSP00000506531.1:p.Asn431Asp
ENST00000679416.1:n.5117A>G
ENST00000679435.1:c.3613A>G	ENSP00000505218.1:p.Asn1205Asp
ENST00000679516.1:c.3613A>G	ENSP00000505187.1:p.Asn1205Asp
ENST00000679618.1:c.*701A>G	ENSP00000506274.1:n.*701A>G
ENST00000679630.1:n.5462A>G
ENST00000679686.1:n.3727A>G
ENST00000679701.1:n.6605A>G
ENST00000679916.1:c.3613A>G	ENSP00000506172.1:p.Asn1205Asp
ENST00000680000.1:c.3613A>G	ENSP00000506173.1:p.Asn1205Asp
ENST00000680135.1:c.*1577A>G	ENSP00000506211.1:n.*1577A>G
ENST00000680149.1:c.3613A>G	ENSP00000506497.1:p.Asn1205Asp
ENST00000680163.1:c.3613A>G	ENSP00000505092.1:p.Asn1205Asp
ENST00000680174.1:n.4304A>G
ENST00000680236.1:c.*674A>G	ENSP00000506212.1:n.*674A>G
ENST00000680497.1:c.3715A>G	ENSP00000505954.1:p.Asn1239Asp
ENST00000680508.1:c.3613A>G	ENSP00000505749.1:p.Asn1205Asp
ENST00000680569.1:c.*1324A>G	ENSP00000505522.1:n.*1324A>G
ENST00000680630.1:n.4045A>G
ENST00000680634.1:n.21-2852A>G
ENST00000680722.1:n.1413A>G
ENST00000680723.1:n.4396A>G
ENST00000680726.1:c.3613A>G	ENSP00000505505.1:p.Asn1205Asp
ENST00000680737.1:n.3884A>G
ENST00000680759.1:c.3613A>G	ENSP00000505848.1:p.Asn1205Asp
ENST00000680814.1:c.3613A>G	ENSP00000505710.1:p.Asn1205Asp
ENST00000680828.1:c.*1185A>G	ENSP00000505249.1:n.*1185A>G
ENST00000680861.1:c.3613A>G	ENSP00000505043.1:p.Asn1205Asp
ENST00000680927.1:c.3613A>G	ENSP00000505473.1:p.Asn1205Asp
ENST00000680939.1:n.3955A>G
ENST00000681152.1:c.3613A>G	ENSP00000505388.1:p.Asn1205Asp
ENST00000681250.1:c.*330A>G	ENSP00000505684.1:n.*330A>G
ENST00000681256.1:c.*1631A>G	ENSP00000505446.1:n.*1631A>G
ENST00000681279.1:n.4381A>G
ENST00000681303.1:c.3613A>G	ENSP00000505576.1:p.Asn1205Asp
ENST00000681307.1:n.4726A>G
ENST00000681461.1:n.4381A>G
ENST00000681495.1:c.1153A>G	ENSP00000506085.1:p.Asn385Asp
ENST00000681558.1:c.1291A>G	ENSP00000505568.1:p.Asn431Asp
ENST00000681619.1:c.3613A>G	ENSP00000505071.1:p.Asn1205Asp
ENST00000681716.1:c.*1324A>G	ENSP00000505078.1:n.*1324A>G
ENST00000681758.1:n.3955A>G
ENST00000681768.1:c.*1277A>G	ENSP00000506311.1:n.*1277A>G
ENST00000681808.1:c.3613A>G	ENSP00000505219.1:p.Asn1205Asp
ENST00000264276.10:c.3613A>G	ENSP00000264276.6:p.Asn1205Asp
ENST00000439495.5:c.1574A>G
ENST00000482891.5:n.3753A>G
ENST00000489440.5:n.434A>G
NM_020919.3:c.3613A>G	NP_065970.2:p.Asn1205Asp
XM_005246709.2:c.3613A>G	XP_005246766.1:p.Asn1205Asp
XM_006712654.1:c.3613A>G	XP_006712717.1:p.Asn1205Asp
XM_006712655.2:c.1549A>G	XP_006712718.1:p.Asn517Asp
XM_011511530.1:c.3274A>G	XP_011509832.1:p.Asn1092Asp
XM_011511531.1:c.3613A>G	XP_011509833.1:p.Asn1205Asp
XR_922974.1:n.3748A>G
XM_006712654.3:c.3613A>G	XP_006712717.1:p.Asn1205Asp
XM_006712655.3:c.1549A>G	XP_006712718.1:p.Asn517Asp
XM_017004569.2:c.3613A>G	XP_016860058.1:p.Asn1205Asp
XM_017004570.2:c.3613A>G	XP_016860059.1:p.Asn1205Asp
XM_017004572.2:c.1231A>G	XP_016860061.1:p.Asn411Asp
XM_024453024.1:c.3274A>G	XP_024308792.1:p.Asn1092Asp
XM_024453025.1:c.1549A>G	XP_024308793.1:p.Asn517Asp
XR_001738864.2:n.3748A>G
XR_001738865.2:n.3748A>G
XR_001738866.2:n.3748A>G
XR_001738867.2:n.3748A>G
XR_002959320.1:n.2804A>G
NM_020919.4:c.3613A>G MANE Select	NP_065970.2:p.Asn1205Asp