Canonical Allele Identifier: CA2155254756
Gene: ATXN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92070641G= , CM000676.2:g.92070641G= GRCh38
NC_000014.8:g.92536985G= , CM000676.1:g.92536985G= GRCh37
NC_000014.7:g.91606738G= NCBI36
NG_008198.2:g.40981C=

Transcript Alleles

HGVS Amino-acid change
ENST00000359366.10:c.*665+294C= ENSP00000352324.5:n.*665+294C=
ENST00000644486.2:c.991+294C= MANE Select ENSP00000496695.1:n.991+294C=
ENST00000647161.1:c.991+294C= ENSP00000493680.1:n.991+294C=
ENST00000340660.10:c.826+294C= ENSP00000339110.6:n.826+294C=
ENST00000359366.9:c.*665+294C= ENSP00000352324.5:n.*665+294C=
ENST00000393287.9:c.838+294C= ENSP00000376965.6:n.838+294C=
ENST00000429774.6:c.781+294C= ENSP00000389376.3:n.781+294C=
ENST00000502250.5:c.454+294C= ENSP00000425322.1:n.454+294C=
ENST00000503767.5:c.946+294C= ENSP00000426697.1:n.946+294C=
ENST00000526245.1:n.117-11854C=
ENST00000545170.5:c.1018+294C= ENSP00000445618.2:n.1018+294C=
ENST00000558190.5:c.991+294C= ENSP00000478320.1:n.991+294C=
ENST00000624063.1:c.26-364G= ENSP00000485197.1:n.26-364G=
NM_001127696.1:c.946+294C= NP_001121168.1:n.946+294C=
NM_001127697.2:c.838+294C= NP_001121169.2:n.838+294C=
NM_001164774.1:c.*41+294C= NP_001158246.1:n.*41+294C=
NM_001164776.1:c.*41+294C= NP_001158248.1:n.*41+294C=
NM_001164777.1:c.*41+294C= NP_001158249.1:n.*41+294C=
NM_001164778.1:c.*41+294C= NP_001158250.1:n.*41+294C=
NM_001164779.1:c.628+294C= NP_001158251.1:n.628+294C=
NM_001164780.1:c.454+294C= NP_001158252.1:n.454+294C=
NM_001164781.1:c.781+294C= NP_001158253.1:n.781+294C=
NM_001164782.1:c.*41+294C= NP_001158254.1:n.*41+294C=
NM_004993.5:c.991+294C= NP_004984.2:n.991+294C=
NM_030660.4:c.826+294C= NP_109376.1:n.826+294C=
NR_028453.1:n.974+294C=
NR_028454.1:n.809+294C=
NR_028455.1:n.1028+294C=
NR_028456.1:n.863+294C=
NR_028457.1:n.1119+294C=
NR_028458.1:n.963+294C=
NR_028459.1:n.1114+294C=
NR_028460.1:n.489+294C=
NR_028461.1:n.972+294C=
NR_028462.1:n.951+294C=
NR_028463.1:n.663+294C=
NR_028464.1:n.961+294C=
NR_028465.1:n.983+294C=
NR_028466.1:n.609+294C=
NR_028467.1:n.975+294C=
NR_028468.1:n.807+294C=
NR_028469.1:n.821+294C=
NR_028470.1:n.279+294C=
NR_031765.1:n.476+294C=
NM_001127696.2:c.946+294C= NP_001121168.1:n.946+294C=
NM_001164774.2:c.*41+294C= NP_001158246.1:n.*41+294C=
NM_001164776.2:c.*41+294C= NP_001158248.1:n.*41+294C=
NM_001164777.2:c.*41+294C= NP_001158249.1:n.*41+294C=
NM_001164778.2:c.*41+294C= NP_001158250.1:n.*41+294C=
NM_001164779.2:c.628+294C= NP_001158251.1:n.628+294C=
NM_001164780.2:c.454+294C= NP_001158252.1:n.454+294C=
NM_001164782.2:c.*41+294C= NP_001158254.1:n.*41+294C=
NM_004993.6:c.991+294C= MANE Select NP_004984.2:n.991+294C=
NM_030660.5:c.826+294C= NP_109376.1:n.826+294C=
NR_028453.2:n.935+294C=
NR_028454.2:n.770+294C=
NR_028455.2:n.989+294C=
NR_028456.2:n.824+294C=
NR_028457.2:n.1080+294C=
NR_028458.2:n.924+294C=
NR_028459.2:n.1075+294C=
NR_028460.2:n.450+294C=
NR_028461.2:n.933+294C=
NR_028462.2:n.912+294C=
NR_028463.2:n.624+294C=
NR_028464.2:n.922+294C=
NR_028465.2:n.944+294C=
NR_028466.2:n.570+294C=
NR_028467.2:n.936+294C=
NR_028468.2:n.768+294C=
NR_028469.2:n.782+294C=
NR_028470.2:n.240+294C=
NR_031765.2:n.437+294C=
NM_001127697.3:c.838+294C= NP_001121169.2:n.838+294C=
NM_001164781.2:c.781+294C= NP_001158253.1:n.781+294C=