Canonical Allele Identifier: CA647660557

Gene: ALS2

Linked Data

• COSMIC: COSN9871585

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201723267A>C , CM000664.2:g.201723267A>C	GRCh38
NC_000002.11:g.202587990A>C , CM000664.1:g.202587990A>C	GRCh37
NC_000002.10:g.202296235A>C	NCBI36
NG_008775.1:g.62906T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264276.11:c.3624+63T>G MANE Select	ENSP00000264276.6:n.3624+63T>G
ENST00000439495.6:c.1302+63T>G	ENSP00000403832.2:n.1302+63T>G
ENST00000482891.6:n.4392+63T>G
ENST00000494017.6:n.1356+63T>G
ENST00000679409.1:c.1302+63T>G	ENSP00000506531.1:n.1302+63T>G
ENST00000679416.1:n.5128+63T>G
ENST00000679435.1:c.3624+63T>G	ENSP00000505218.1:n.3624+63T>G
ENST00000679516.1:c.3624+63T>G	ENSP00000505187.1:n.3624+63T>G
ENST00000679618.1:c.*712+63T>G	ENSP00000506274.1:n.*712+63T>G
ENST00000679630.1:n.5473+63T>G
ENST00000679686.1:n.3738+63T>G
ENST00000679701.1:n.6616+63T>G
ENST00000679916.1:c.3624+63T>G	ENSP00000506172.1:n.3624+63T>G
ENST00000680000.1:c.3624+63T>G	ENSP00000506173.1:n.3624+63T>G
ENST00000680135.1:c.*1588+63T>G	ENSP00000506211.1:n.*1588+63T>G
ENST00000680149.1:c.3624+63T>G	ENSP00000506497.1:n.3624+63T>G
ENST00000680163.1:c.3624+63T>G	ENSP00000505092.1:n.3624+63T>G
ENST00000680174.1:n.4315+63T>G
ENST00000680236.1:c.*685+63T>G	ENSP00000506212.1:n.*685+63T>G
ENST00000680497.1:c.3726+63T>G	ENSP00000505954.1:n.3726+63T>G
ENST00000680508.1:c.3624+63T>G	ENSP00000505749.1:n.3624+63T>G
ENST00000680569.1:c.*1335+63T>G	ENSP00000505522.1:n.*1335+63T>G
ENST00000680630.1:n.4056+63T>G
ENST00000680634.1:n.21-2778T>G
ENST00000680722.1:n.1424+63T>G
ENST00000680723.1:n.4407+63T>G
ENST00000680726.1:c.3624+63T>G	ENSP00000505505.1:n.3624+63T>G
ENST00000680737.1:n.3895+63T>G
ENST00000680759.1:c.3624+63T>G	ENSP00000505848.1:n.3624+63T>G
ENST00000680814.1:c.3624+63T>G	ENSP00000505710.1:n.3624+63T>G
ENST00000680828.1:c.*1196+63T>G	ENSP00000505249.1:n.*1196+63T>G
ENST00000680861.1:c.3624+63T>G	ENSP00000505043.1:n.3624+63T>G
ENST00000680927.1:c.3624+63T>G	ENSP00000505473.1:n.3624+63T>G
ENST00000680939.1:n.3966+63T>G
ENST00000681152.1:c.3624+63T>G	ENSP00000505388.1:n.3624+63T>G
ENST00000681250.1:c.*341+63T>G	ENSP00000505684.1:n.*341+63T>G
ENST00000681256.1:c.*1642+63T>G	ENSP00000505446.1:n.*1642+63T>G
ENST00000681279.1:n.4392+63T>G
ENST00000681303.1:c.3624+63T>G	ENSP00000505576.1:n.3624+63T>G
ENST00000681307.1:n.4737+63T>G
ENST00000681461.1:n.4392+63T>G
ENST00000681495.1:c.1164+63T>G	ENSP00000506085.1:n.1164+63T>G
ENST00000681558.1:c.1302+63T>G	ENSP00000505568.1:n.1302+63T>G
ENST00000681619.1:c.3624+63T>G	ENSP00000505071.1:n.3624+63T>G
ENST00000681716.1:c.*1335+63T>G	ENSP00000505078.1:n.*1335+63T>G
ENST00000681758.1:n.3966+63T>G
ENST00000681768.1:c.*1288+63T>G	ENSP00000506311.1:n.*1288+63T>G
ENST00000681808.1:c.3624+63T>G	ENSP00000505219.1:n.3624+63T>G
ENST00000264276.10:c.3624+63T>G	ENSP00000264276.6:n.3624+63T>G
ENST00000439495.5:c.1585+63T>G
ENST00000482891.5:n.3764+63T>G
ENST00000489440.5:n.445+63T>G
NM_020919.3:c.3624+63T>G	NP_065970.2:n.3624+63T>G
XM_005246709.2:c.3624+63T>G	XP_005246766.1:n.3624+63T>G
XM_006712654.1:c.3624+63T>G	XP_006712717.1:n.3624+63T>G
XM_006712655.2:c.1560+63T>G	XP_006712718.1:n.1560+63T>G
XM_011511530.1:c.3285+63T>G	XP_011509832.1:n.3285+63T>G
XM_011511531.1:c.3624+63T>G	XP_011509833.1:n.3624+63T>G
XR_922974.1:n.3759+63T>G
XM_006712654.3:c.3624+63T>G	XP_006712717.1:n.3624+63T>G
XM_006712655.3:c.1560+63T>G	XP_006712718.1:n.1560+63T>G
XM_017004569.2:c.3624+63T>G	XP_016860058.1:n.3624+63T>G
XM_017004570.2:c.3624+63T>G	XP_016860059.1:n.3624+63T>G
XM_017004572.2:c.1242+63T>G	XP_016860061.1:n.1242+63T>G
XM_024453024.1:c.3285+63T>G	XP_024308792.1:n.3285+63T>G
XM_024453025.1:c.1560+63T>G	XP_024308793.1:n.1560+63T>G
XR_001738864.2:n.3759+63T>G
XR_001738865.2:n.3759+63T>G
XR_001738866.2:n.3759+63T>G
XR_001738867.2:n.3759+63T>G
XR_002959320.1:n.2815+63T>G
NM_020919.4:c.3624+63T>G MANE Select	NP_065970.2:n.3624+63T>G