Canonical Allele Identifier: CA1612705075
Gene: ATXN1 HGNC NCBI

Linked Data

dbSNP Id: rs1758457073

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.16396245T>C , CM000668.2:g.16396245T>C GRCh38
NC_000006.11:g.16396476T>C , CM000668.1:g.16396476T>C GRCh37
NC_000006.10:g.16504455T>C NCBI36
NG_011571.1:g.370246A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000436367.6:c.-160-67775A>G MANE Select ENSP00000416360.1:n.-160-67775A>G
ENST00000244769.8:c.-160-67775A>G ENSP00000244769.3:n.-160-67775A>G
ENST00000436367.5:c.-160-67775A>G ENSP00000416360.1:n.-160-67775A>G
NM_000332.3:c.-160-67775A>G NP_000323.2:n.-160-67775A>G
NM_001128164.1:c.-160-67775A>G NP_001121636.1:n.-160-67775A>G
NM_001357857.1:c.-189-67775A>G NP_001344786.1:n.-189-67775A>G
NM_001357857.2:c.-189-67775A>G NP_001344786.1:n.-189-67775A>G
NM_001128164.2:c.-160-67775A>G MANE Select NP_001121636.1:n.-160-67775A>G
NM_000332.4:c.-160-67775A>G NP_000323.2:n.-160-67775A>G