Canonical Allele Identifier: CA134935594
Gene: ATXN1 HGNC NCBI

Linked Data

dbSNP Id: rs996037178
MyVariant Identifiers: chr6:g.16396552A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.16396552A>T , CM000668.2:g.16396552A>T GRCh38
NC_000006.11:g.16396783A>T , CM000668.1:g.16396783A>T GRCh37
NC_000006.10:g.16504762A>T NCBI36
NG_011571.1:g.369939T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000436367.6:c.-160-68082T>A MANE Select ENSP00000416360.1:n.-160-68082T>A
ENST00000244769.8:c.-160-68082T>A ENSP00000244769.3:n.-160-68082T>A
ENST00000436367.5:c.-160-68082T>A ENSP00000416360.1:n.-160-68082T>A
NM_000332.3:c.-160-68082T>A NP_000323.2:n.-160-68082T>A
NM_001128164.1:c.-160-68082T>A NP_001121636.1:n.-160-68082T>A
NM_001357857.1:c.-189-68082T>A NP_001344786.1:n.-189-68082T>A
NM_001357857.2:c.-189-68082T>A NP_001344786.1:n.-189-68082T>A
NM_001128164.2:c.-160-68082T>A MANE Select NP_001121636.1:n.-160-68082T>A
NM_000332.4:c.-160-68082T>A NP_000323.2:n.-160-68082T>A
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