Canonical Allele Identifier: CA2662673976

Gene: ALS2

Linked Data

• gnomAD v4: 2-201704064-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201704065del , CM000664.2:g.201704065del	GRCh38
NC_000002.11:g.202568788del , CM000664.1:g.202568788del	GRCh37
NC_000002.10:g.202277033del	NCBI36
NG_008775.1:g.82108del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264276.11:c.4935+57del MANE Select	ENSP00000264276.6:n.4935+57del
ENST00000439495.6:c.*1115+57del	ENSP00000403832.2:n.*1115+57del
ENST00000679409.1:c.*1697del	ENSP00000506531.1:n.*1697del
ENST00000679416.1:n.6439+57del
ENST00000679427.1:n.2663del
ENST00000679435.1:c.4935+57del	ENSP00000505218.1:n.4935+57del
ENST00000679516.1:c.4935+57del	ENSP00000505187.1:n.4935+57del
ENST00000679618.1:c.*2023+57del	ENSP00000506274.1:n.*2023+57del
ENST00000679630.1:n.6784+57del
ENST00000679635.1:n.3197+57del
ENST00000679686.1:n.5049+57del
ENST00000679701.1:n.7927+57del
ENST00000679916.1:c.*1283+57del	ENSP00000506172.1:n.*1283+57del
ENST00000680000.1:c.*36del	ENSP00000506173.1:n.*36del
ENST00000680135.1:c.*2896+57del	ENSP00000506211.1:n.*2896+57del
ENST00000680149.1:c.*217+57del	ENSP00000506497.1:n.*217+57del
ENST00000680163.1:c.4935+57del	ENSP00000505092.1:n.4935+57del
ENST00000680174.1:n.5626+57del
ENST00000680236.1:c.*1996+57del	ENSP00000506212.1:n.*1996+57del
ENST00000680404.1:n.507del
ENST00000680441.1:n.3493+57del
ENST00000680497.1:c.5037+57del	ENSP00000505954.1:n.5037+57del
ENST00000680508.1:c.*91+57del	ENSP00000505749.1:n.*91+57del
ENST00000680569.1:c.*2878+57del	ENSP00000505522.1:n.*2878+57del
ENST00000680634.1:n.1443+57del
ENST00000680722.1:n.2735+57del
ENST00000680726.1:c.*217+57del	ENSP00000505505.1:n.*217+57del
ENST00000680759.1:c.4767+57del	ENSP00000505848.1:n.4767+57del
ENST00000680814.1:c.4838+389del	ENSP00000505710.1:n.4838+389del
ENST00000680828.1:c.*2629+57del	ENSP00000505249.1:n.*2629+57del
ENST00000680861.1:c.4935+57del	ENSP00000505043.1:n.4935+57del
ENST00000680927.1:c.*1115+57del	ENSP00000505473.1:n.*1115+57del
ENST00000680939.1:n.6933del
ENST00000681250.1:c.*1652+57del	ENSP00000505684.1:n.*1652+57del
ENST00000681256.1:c.*2950+57del	ENSP00000505446.1:n.*2950+57del
ENST00000681279.1:n.5801+57del
ENST00000681307.1:n.6048+57del
ENST00000681461.1:n.5703+57del
ENST00000681495.1:c.2472+57del	ENSP00000506085.1:n.2472+57del
ENST00000681558.1:c.2613+57del	ENSP00000505568.1:n.2613+57del
ENST00000681619.1:c.4932+57del	ENSP00000505071.1:n.4932+57del
ENST00000681663.1:n.1841+57del
ENST00000681692.1:n.2895+57del
ENST00000681716.1:c.*2789+57del	ENSP00000505078.1:n.*2789+57del
ENST00000681768.1:c.*2599+57del	ENSP00000506311.1:n.*2599+57del
ENST00000681808.1:c.4758+57del	ENSP00000505219.1:n.4758+57del
ENST00000264276.10:c.4935+57del	ENSP00000264276.6:n.4935+57del
ENST00000439495.5:c.3039+57del
NM_020919.3:c.4935+57del	NP_065970.2:n.4935+57del
XM_005246709.2:c.4932+57del	XP_005246766.1:n.4932+57del
XM_006712654.1:c.4935+57del	XP_006712717.1:n.4935+57del
XM_006712655.2:c.2871+57del	XP_006712718.1:n.2871+57del
XM_011511530.1:c.4596+57del	XP_011509832.1:n.4596+57del
XR_922974.1:n.5213+57del
XM_006712654.3:c.4935+57del	XP_006712717.1:n.4935+57del
XM_006712655.3:c.2871+57del	XP_006712718.1:n.2871+57del
XM_017004569.2:c.4932+57del	XP_016860058.1:n.4932+57del
XM_017004572.2:c.2553+57del	XP_016860061.1:n.2553+57del
XM_024453024.1:c.4596+57del	XP_024308792.1:n.4596+57del
XM_024453025.1:c.2868+57del	XP_024308793.1:n.2868+57del
XR_001738864.2:n.5050+57del
XR_001738865.2:n.5047+57del
XR_001738866.2:n.5213+57del
XR_001738867.2:n.5210+57del
XR_002959320.1:n.4106+57del
NM_020919.4:c.4935+57del MANE Select	NP_065970.2:n.4935+57del