Canonical Allele Identifier: CA2662676402

Gene: ALS2

Linked Data

• gnomAD v4: 2-201722983-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201722983_201722984insG , CM000664.2:g.201722983_201722984insG	GRCh38
NC_000002.11:g.202587706_202587707insG , CM000664.1:g.202587706_202587707insG	GRCh37
NC_000002.10:g.202295951_202295952insG	NCBI36
NG_008775.1:g.63189_63190insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264276.11:c.3702+59_3702+60insC MANE Select	ENSP00000264276.6:n.3702+59_3702+60insC
ENST00000439495.6:c.1380+59_1380+60insC	ENSP00000403832.2:n.1380+59_1380+60insC
ENST00000482891.6:n.4529_4530insC
ENST00000494017.6:n.1493_1494insC
ENST00000679409.1:c.1380+59_1380+60insC	ENSP00000506531.1:n.1380+59_1380+60insC
ENST00000679416.1:n.5206+59_5206+60insC
ENST00000679435.1:c.3702+59_3702+60insC	ENSP00000505218.1:n.3702+59_3702+60insC
ENST00000679516.1:c.3702+59_3702+60insC	ENSP00000505187.1:n.3702+59_3702+60insC
ENST00000679618.1:c.*790+59_*790+60insC	ENSP00000506274.1:n.*790+59_*790+60insC
ENST00000679630.1:n.5551+59_5551+60insC
ENST00000679686.1:n.3816+59_3816+60insC
ENST00000679701.1:n.6694+59_6694+60insC
ENST00000679916.1:c.3702+59_3702+60insC	ENSP00000506172.1:n.3702+59_3702+60insC
ENST00000680000.1:c.3702+59_3702+60insC	ENSP00000506173.1:n.3702+59_3702+60insC
ENST00000680135.1:c.*1666+59_*1666+60insC	ENSP00000506211.1:n.*1666+59_*1666+60insC
ENST00000680149.1:c.3702+59_3702+60insC	ENSP00000506497.1:n.3702+59_3702+60insC
ENST00000680163.1:c.3702+59_3702+60insC	ENSP00000505092.1:n.3702+59_3702+60insC
ENST00000680174.1:n.4393+59_4393+60insC
ENST00000680236.1:c.*763+59_*763+60insC	ENSP00000506212.1:n.*763+59_*763+60insC
ENST00000680497.1:c.3804+59_3804+60insC	ENSP00000505954.1:n.3804+59_3804+60insC
ENST00000680508.1:c.3702+59_3702+60insC	ENSP00000505749.1:n.3702+59_3702+60insC
ENST00000680569.1:c.*1413+59_*1413+60insC	ENSP00000505522.1:n.*1413+59_*1413+60insC
ENST00000680630.1:n.4134+59_4134+60insC
ENST00000680634.1:n.21-2495_21-2494insC
ENST00000680722.1:n.1502+59_1502+60insC
ENST00000680723.1:n.4544_4545insC
ENST00000680726.1:c.3702+59_3702+60insC	ENSP00000505505.1:n.3702+59_3702+60insC
ENST00000680737.1:n.3973+59_3973+60insC
ENST00000680759.1:c.3702+59_3702+60insC	ENSP00000505848.1:n.3702+59_3702+60insC
ENST00000680814.1:c.3702+59_3702+60insC	ENSP00000505710.1:n.3702+59_3702+60insC
ENST00000680828.1:c.*1274+59_*1274+60insC	ENSP00000505249.1:n.*1274+59_*1274+60insC
ENST00000680861.1:c.3702+59_3702+60insC	ENSP00000505043.1:n.3702+59_3702+60insC
ENST00000680927.1:c.3702+59_3702+60insC	ENSP00000505473.1:n.3702+59_3702+60insC
ENST00000680939.1:n.4044+59_4044+60insC
ENST00000681152.1:c.*47_*48insC	ENSP00000505388.1:n.*47_*48insC
ENST00000681250.1:c.*419+59_*419+60insC	ENSP00000505684.1:n.*419+59_*419+60insC
ENST00000681256.1:c.*1720+59_*1720+60insC	ENSP00000505446.1:n.*1720+59_*1720+60insC
ENST00000681279.1:n.4470+59_4470+60insC
ENST00000681303.1:c.*47_*48insC	ENSP00000505576.1:n.*47_*48insC
ENST00000681307.1:n.4815+59_4815+60insC
ENST00000681461.1:n.4470+59_4470+60insC
ENST00000681495.1:c.1242+59_1242+60insC	ENSP00000506085.1:n.1242+59_1242+60insC
ENST00000681558.1:c.1380+59_1380+60insC	ENSP00000505568.1:n.1380+59_1380+60insC
ENST00000681619.1:c.3702+59_3702+60insC	ENSP00000505071.1:n.3702+59_3702+60insC
ENST00000681716.1:c.*1413+59_*1413+60insC	ENSP00000505078.1:n.*1413+59_*1413+60insC
ENST00000681758.1:n.4044+59_4044+60insC
ENST00000681768.1:c.*1366+59_*1366+60insC	ENSP00000506311.1:n.*1366+59_*1366+60insC
ENST00000681808.1:c.3702+59_3702+60insC	ENSP00000505219.1:n.3702+59_3702+60insC
ENST00000264276.10:c.3702+59_3702+60insC	ENSP00000264276.6:n.3702+59_3702+60insC
ENST00000439495.5:c.1663+59_1663+60insC
ENST00000482891.5:n.3901_3902insC
ENST00000489440.5:n.523+59_523+60insC
NM_020919.3:c.3702+59_3702+60insC	NP_065970.2:n.3702+59_3702+60insC
XM_005246709.2:c.3702+59_3702+60insC	XP_005246766.1:n.3702+59_3702+60insC
XM_006712654.1:c.3702+59_3702+60insC	XP_006712717.1:n.3702+59_3702+60insC
XM_006712655.2:c.1638+59_1638+60insC	XP_006712718.1:n.1638+59_1638+60insC
XM_011511530.1:c.3363+59_3363+60insC	XP_011509832.1:n.3363+59_3363+60insC
XM_011511531.1:c.3702+59_3702+60insC	XP_011509833.1:n.3702+59_3702+60insC
XR_922974.1:n.3837+59_3837+60insC
XM_006712654.3:c.3702+59_3702+60insC	XP_006712717.1:n.3702+59_3702+60insC
XM_006712655.3:c.1638+59_1638+60insC	XP_006712718.1:n.1638+59_1638+60insC
XM_017004569.2:c.3702+59_3702+60insC	XP_016860058.1:n.3702+59_3702+60insC
XM_017004570.2:c.3702+59_3702+60insC	XP_016860059.1:n.3702+59_3702+60insC
XM_017004572.2:c.1320+59_1320+60insC	XP_016860061.1:n.1320+59_1320+60insC
XM_024453024.1:c.3363+59_3363+60insC	XP_024308792.1:n.3363+59_3363+60insC
XM_024453025.1:c.1638+59_1638+60insC	XP_024308793.1:n.1638+59_1638+60insC
XR_001738864.2:n.3837+59_3837+60insC
XR_001738865.2:n.3837+59_3837+60insC
XR_001738866.2:n.3837+59_3837+60insC
XR_001738867.2:n.3837+59_3837+60insC
XR_002959320.1:n.2893+59_2893+60insC
NM_020919.4:c.3702+59_3702+60insC MANE Select	NP_065970.2:n.3702+59_3702+60insC