Canonical Allele Identifier: CA1321201134

Gene: ALS2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201767196A= , CM000664.2:g.201767196A=	GRCh38
NC_000002.11:g.202631919A= , CM000664.1:g.202631919A=	GRCh37
NC_000002.10:g.202340164A=	NCBI36
NG_008775.1:g.18977T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264276.11:c.175+33T= MANE Select	ENSP00000264276.6:n.175+33T=
ENST00000409632.7:c.175+33T=	ENSP00000386384.3:n.175+33T=
ENST00000482789.6:n.517+33T=
ENST00000482891.6:n.517+33T=
ENST00000679416.1:n.517+33T=
ENST00000679435.1:c.175+33T=	ENSP00000505218.1:n.175+33T=
ENST00000679503.1:c.175+33T=	ENSP00000505968.1:n.175+33T=
ENST00000679516.1:c.175+33T=	ENSP00000505187.1:n.175+33T=
ENST00000679550.1:c.175+33T=	ENSP00000506193.1:n.175+33T=
ENST00000679618.1:c.175+33T=	ENSP00000506274.1:n.175+33T=
ENST00000679630.1:n.517+33T=
ENST00000679686.1:n.289+33T=
ENST00000679701.1:n.517+33T=
ENST00000679728.1:c.175+33T=	ENSP00000504981.1:n.175+33T=
ENST00000679916.1:c.175+33T=	ENSP00000506172.1:n.175+33T=
ENST00000679939.1:c.175+33T=	ENSP00000505704.1:n.175+33T=
ENST00000679949.1:c.175+33T=	ENSP00000505232.1:n.175+33T=
ENST00000680000.1:c.175+33T=	ENSP00000506173.1:n.175+33T=
ENST00000680135.1:c.175+33T=	ENSP00000506211.1:n.175+33T=
ENST00000680149.1:c.175+33T=	ENSP00000506497.1:n.175+33T=
ENST00000680163.1:c.175+33T=	ENSP00000505092.1:n.175+33T=
ENST00000680174.1:n.517+33T=
ENST00000680188.1:c.175+33T=	ENSP00000505665.1:n.175+33T=
ENST00000680236.1:c.175+33T=	ENSP00000506212.1:n.175+33T=
ENST00000680287.1:c.175+33T=	ENSP00000506547.1:n.175+33T=
ENST00000680497.1:c.175+33T=	ENSP00000505954.1:n.175+33T=
ENST00000680508.1:c.175+33T=	ENSP00000505749.1:n.175+33T=
ENST00000680569.1:c.175+33T=	ENSP00000505522.1:n.175+33T=
ENST00000680630.1:n.517+33T=
ENST00000680644.1:c.175+33T=	ENSP00000505738.1:n.175+33T=
ENST00000680726.1:c.175+33T=	ENSP00000505505.1:n.175+33T=
ENST00000680737.1:n.517+33T=
ENST00000680759.1:c.175+33T=	ENSP00000505848.1:n.175+33T=
ENST00000680814.1:c.175+33T=	ENSP00000505710.1:n.175+33T=
ENST00000680828.1:c.175+33T=	ENSP00000505249.1:n.175+33T=
ENST00000680861.1:c.175+33T=	ENSP00000505043.1:n.175+33T=
ENST00000680927.1:c.175+33T=	ENSP00000505473.1:n.175+33T=
ENST00000680939.1:n.517+33T=
ENST00000681144.1:c.175+33T=	ENSP00000505348.1:n.175+33T=
ENST00000681152.1:c.175+33T=	ENSP00000505388.1:n.175+33T=
ENST00000681250.1:c.175+33T=	ENSP00000505684.1:n.175+33T=
ENST00000681256.1:c.175+33T=	ENSP00000505446.1:n.175+33T=
ENST00000681279.1:n.517+33T=
ENST00000681303.1:c.175+33T=	ENSP00000505576.1:n.175+33T=
ENST00000681307.1:n.517+33T=
ENST00000681312.1:c.175+33T=	ENSP00000506656.1:n.175+33T=
ENST00000681378.1:n.517+33T=
ENST00000681461.1:n.517+33T=
ENST00000681619.1:c.175+33T=	ENSP00000505071.1:n.175+33T=
ENST00000681716.1:c.175+33T=	ENSP00000505078.1:n.175+33T=
ENST00000681758.1:n.517+33T=
ENST00000681768.1:c.175+33T=	ENSP00000506311.1:n.175+33T=
ENST00000681808.1:c.175+33T=	ENSP00000505219.1:n.175+33T=
ENST00000264276.10:c.175+33T=	ENSP00000264276.6:n.175+33T=
ENST00000409632.6:c.175+33T=	ENSP00000386384.2:n.175+33T=
ENST00000410052.1:c.175+33T=	ENSP00000386948.1:n.175+33T=
ENST00000462747.1:n.270+33T=
ENST00000467448.5:c.175+33T=	ENSP00000429223.1:n.175+33T=
ENST00000482789.5:n.315+33T=
ENST00000482891.5:n.315+33T=
ENST00000496244.5:n.315+33T=
NM_001135745.1:c.175+33T=	NP_001129217.1:n.175+33T=
NM_020919.3:c.175+33T=	NP_065970.2:n.175+33T=
XM_005246709.2:c.175+33T=	XP_005246766.1:n.175+33T=
XM_006712654.1:c.175+33T=	XP_006712717.1:n.175+33T=
XM_011511530.1:c.-340+33T=	XP_011509832.1:n.-340+33T=
XM_011511531.1:c.175+33T=	XP_011509833.1:n.175+33T=
XR_922974.1:n.310+33T=
XM_006712654.3:c.175+33T=	XP_006712717.1:n.175+33T=
XM_017004569.2:c.175+33T=	XP_016860058.1:n.175+33T=
XM_017004570.2:c.175+33T=	XP_016860059.1:n.175+33T=
XM_024453024.1:c.-340+33T=	XP_024308792.1:n.-340+33T=
XR_001738864.2:n.310+33T=
XR_001738865.2:n.310+33T=
XR_001738866.2:n.310+33T=
XR_001738867.2:n.310+33T=
NM_020919.4:c.175+33T= MANE Select	NP_065970.2:n.175+33T=
NM_001135745.2:c.175+33T=	NP_001129217.1:n.175+33T=