Canonical Allele Identifier: CA1321156539
Gene: ALS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201704232A= , CM000664.2:g.201704232A= GRCh38
NC_000002.11:g.202568955A= , CM000664.1:g.202568955A= GRCh37
NC_000002.10:g.202277200A= NCBI36
NG_008775.1:g.81941T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264276.11:c.4839-14T= MANE Select ENSP00000264276.6:n.4839-14T=
ENST00000439495.6:c.*1019-14T= ENSP00000403832.2:n.*1019-14T=
ENST00000679409.1:c.*1530T= ENSP00000506531.1:n.*1530T=
ENST00000679416.1:n.6343-14T=
ENST00000679427.1:n.2496T=
ENST00000679435.1:c.4839-14T= ENSP00000505218.1:n.4839-14T=
ENST00000679516.1:c.4839-14T= ENSP00000505187.1:n.4839-14T=
ENST00000679618.1:c.*1927-14T= ENSP00000506274.1:n.*1927-14T=
ENST00000679630.1:n.6688-14T=
ENST00000679635.1:n.3087T=
ENST00000679686.1:n.4953-14T=
ENST00000679701.1:n.7831-14T=
ENST00000679916.1:c.*1187-14T= ENSP00000506172.1:n.*1187-14T=
ENST00000680000.1:c.4839-14T= ENSP00000506173.1:n.4839-14T=
ENST00000680135.1:c.*2800-14T= ENSP00000506211.1:n.*2800-14T=
ENST00000680149.1:c.*121-14T= ENSP00000506497.1:n.*121-14T=
ENST00000680163.1:c.4839-14T= ENSP00000505092.1:n.4839-14T=
ENST00000680174.1:n.5530-14T=
ENST00000680236.1:c.*1900-14T= ENSP00000506212.1:n.*1900-14T=
ENST00000680404.1:n.354-14T=
ENST00000680441.1:n.3397-14T=
ENST00000680497.1:c.4941-14T= ENSP00000505954.1:n.4941-14T=
ENST00000680508.1:c.4844T= ENSP00000505749.1:p.Phe1615=
ENST00000680569.1:c.*2768T= ENSP00000505522.1:n.*2768T=
ENST00000680634.1:n.1347-14T=
ENST00000680722.1:n.2639-14T=
ENST00000680726.1:c.*121-14T= ENSP00000505505.1:n.*121-14T=
ENST00000680759.1:c.4671-14T= ENSP00000505848.1:n.4671-14T=
ENST00000680814.1:c.4838+222T= ENSP00000505710.1:n.4838+222T=
ENST00000680828.1:c.*2533-14T= ENSP00000505249.1:n.*2533-14T=
ENST00000680861.1:c.4839-14T= ENSP00000505043.1:n.4839-14T=
ENST00000680927.1:c.*1019-14T= ENSP00000505473.1:n.*1019-14T=
ENST00000680939.1:n.6766T=
ENST00000681250.1:c.*1556-14T= ENSP00000505684.1:n.*1556-14T=
ENST00000681256.1:c.*2854-14T= ENSP00000505446.1:n.*2854-14T=
ENST00000681279.1:n.5705-14T=
ENST00000681307.1:n.5952-14T=
ENST00000681461.1:n.5607-14T=
ENST00000681495.1:c.2376-14T= ENSP00000506085.1:n.2376-14T=
ENST00000681558.1:c.2517-14T= ENSP00000505568.1:n.2517-14T=
ENST00000681619.1:c.4836-14T= ENSP00000505071.1:n.4836-14T=
ENST00000681663.1:n.1745-14T=
ENST00000681692.1:n.2799-14T=
ENST00000681716.1:c.*2693-14T= ENSP00000505078.1:n.*2693-14T=
ENST00000681768.1:c.*2503-14T= ENSP00000506311.1:n.*2503-14T=
ENST00000681808.1:c.4662-14T= ENSP00000505219.1:n.4662-14T=
ENST00000264276.10:c.4839-14T= ENSP00000264276.6:n.4839-14T=
ENST00000439495.5:c.2943-14T=
NM_020919.3:c.4839-14T= NP_065970.2:n.4839-14T=
XM_005246709.2:c.4836-14T= XP_005246766.1:n.4836-14T=
XM_006712654.1:c.4839-14T= XP_006712717.1:n.4839-14T=
XM_006712655.2:c.2775-14T= XP_006712718.1:n.2775-14T=
XM_011511530.1:c.4500-14T= XP_011509832.1:n.4500-14T=
XR_922974.1:n.5117-14T=
XM_006712654.3:c.4839-14T= XP_006712717.1:n.4839-14T=
XM_006712655.3:c.2775-14T= XP_006712718.1:n.2775-14T=
XM_017004569.2:c.4836-14T= XP_016860058.1:n.4836-14T=
XM_017004572.2:c.2457-14T= XP_016860061.1:n.2457-14T=
XM_024453024.1:c.4500-14T= XP_024308792.1:n.4500-14T=
XM_024453025.1:c.2772-14T= XP_024308793.1:n.2772-14T=
XR_001738864.2:n.4954-14T=
XR_001738865.2:n.4951-14T=
XR_001738866.2:n.5117-14T=
XR_001738867.2:n.5114-14T=
XR_002959320.1:n.4010-14T=
NM_020919.4:c.4839-14T= MANE Select NP_065970.2:n.4839-14T=