Canonical Allele Identifier: CA2063363639
Gene: ATXN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111569932_111569935delinsTGAA , CM000674.2:g.111569932_111569935delinsTGAA GRCh38
NC_000012.11:g.112007736_112007739delinsTGAA , CM000674.1:g.112007736_112007739delinsTGAA GRCh37
NC_000012.10:g.110492119_110492122delinsTGAA NCBI36
NG_011572.1:g.34742_34745delinsTTCA
NG_011572.2:g.34742_34745delinsTTCA
NG_011572.3:g.34742_34745delinsTTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000389153.10:c.252-14016_252-14013delinsTTCA ENSP00000373805.6:n.252-14016_252-14013delinsTTCA
ENST00000483311.6:c.252-14016_252-14013delinsTTCA ENSP00000446512.2:n.252-14016_252-14013delinsTTCA
ENST00000642389.2:c.252-14016_252-14013delinsTTCA ENSP00000496055.2:n.252-14016_252-14013delinsTTCA
ENST00000643669.2:c.252-14016_252-14013delinsTTCA ENSP00000494663.1:n.252-14016_252-14013delinsTTCA
ENST00000644883.1:c.252-14016_252-14013delinsTTCA ENSP00000496279.1:n.252-14016_252-14013delinsTTCA
ENST00000647305.1:c.252-14016_252-14013delinsTTCA ENSP00000493897.1:n.252-14016_252-14013delinsTTCA
ENST00000671792.1:c.91-14016_91-14013delinsTTCA
ENST00000672105.1:n.74-14016_74-14013delinsTTCA
ENST00000672335.1:n.405-14016_405-14013delinsTTCA
ENST00000672613.1:c.252-14016_252-14013delinsTTCA ENSP00000500649.1:n.252-14016_252-14013delinsTTCA
ENST00000673283.1:c.252-14016_252-14013delinsTTCA ENSP00000500313.1:n.252-14016_252-14013delinsTTCA
ENST00000673436.1:c.252-14016_252-14013delinsTTCA MANE Select ENSP00000500925.1:n.252-14016_252-14013delinsTTCA
ENST00000673449.1:c.252-14016_252-14013delinsTTCA ENSP00000500646.1:n.252-14016_252-14013delinsTTCA
ENST00000673557.1:c.252-14016_252-14013delinsTTCA ENSP00000500766.1:n.252-14016_252-14013delinsTTCA
ENST00000377617.7:c.732-14016_732-14013delinsTTCA ENSP00000366843.3:n.732-14016_732-14013delinsTTCA
ENST00000389153.8:c.-64-14016_-64-14013delinsTTCA ENSP00000373805.4:n.-64-14016_-64-14013delinsTTCA
ENST00000392645.6:n.652-14016_652-14013delinsTTCA
ENST00000483311.5:c.494-14016_494-14013delinsTTCA
ENST00000535949.5:c.-27-15718_-27-15715delinsTTCA ENSP00000439338.1:n.-27-15718_-27-15715delinsTTCA
ENST00000542287.6:c.-64-14016_-64-14013delinsTTCA ENSP00000445583.2:n.-64-14016_-64-14013delinsTTCA
ENST00000548492.1:c.58-16958_58-16955delinsTTCA ENSP00000449566.1:n.58-16958_58-16955delinsTTCA
ENST00000549455.1:n.279+28849_279+28852delinsTTCA
ENST00000550104.5:c.732-14016_732-14013delinsTTCA ENSP00000446576.2:n.732-14016_732-14013delinsTTCA
ENST00000608853.5:c.252-14016_252-14013delinsTTCA ENSP00000476504.1:n.252-14016_252-14013delinsTTCA
ENST00000616825.4:c.-64-14016_-64-14013delinsTTCA ENSP00000481448.1:n.-64-14016_-64-14013delinsTTCA
NM_001310121.1:c.-64-14016_-64-14013delinsTTCA NP_001297050.1:n.-64-14016_-64-14013delinsTTCA
NM_001310123.1:c.-27-15718_-27-15715delinsTTCA NP_001297052.1:n.-27-15718_-27-15715delinsTTCA
NM_002973.3:c.732-14016_732-14013delinsTTCA NP_002964.3:n.732-14016_732-14013delinsTTCA
NR_132311.1:n.894-14016_894-14013delinsTTCA
NM_001372574.1:c.252-14016_252-14013delinsTTCA MANE Select NP_001359503.1:n.252-14016_252-14013delinsTTCA
NM_002973.4:c.252-14016_252-14013delinsTTCA NP_002964.4:n.252-14016_252-14013delinsTTCA
NR_132311.2:n.533-14016_533-14013delinsTTCA