Canonical Allele Identifier: CA134935454
Gene: ATXN1 HGNC NCBI

Linked Data

dbSNP Id: rs179945

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.16396238C>T , CM000668.2:g.16396238C>T GRCh38
NC_000006.11:g.16396469C>T , CM000668.1:g.16396469C>T GRCh37
NC_000006.10:g.16504448C>T NCBI36
NG_011571.1:g.370253G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000436367.6:c.-160-67768G>A MANE Select ENSP00000416360.1:n.-160-67768G>A
ENST00000244769.8:c.-160-67768G>A ENSP00000244769.3:n.-160-67768G>A
ENST00000436367.5:c.-160-67768G>A ENSP00000416360.1:n.-160-67768G>A
NM_000332.3:c.-160-67768G>A NP_000323.2:n.-160-67768G>A
NM_001128164.1:c.-160-67768G>A NP_001121636.1:n.-160-67768G>A
NM_001357857.1:c.-189-67768G>A NP_001344786.1:n.-189-67768G>A
NM_001357857.2:c.-189-67768G>A NP_001344786.1:n.-189-67768G>A
NM_001128164.2:c.-160-67768G>A MANE Select NP_001121636.1:n.-160-67768G>A
NM_000332.4:c.-160-67768G>A NP_000323.2:n.-160-67768G>A