Canonical Allele Identifier: CA1612740117
Gene: ATXN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.16395982T= , CM000668.2:g.16395982T= GRCh38
NC_000006.11:g.16396213T= , CM000668.1:g.16396213T= GRCh37
NC_000006.10:g.16504192T= NCBI36
NG_011571.1:g.370509A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000436367.6:c.-160-67512A= MANE Select ENSP00000416360.1:n.-160-67512A=
ENST00000244769.8:c.-160-67512A= ENSP00000244769.3:n.-160-67512A=
ENST00000436367.5:c.-160-67512A= ENSP00000416360.1:n.-160-67512A=
NM_000332.3:c.-160-67512A= NP_000323.2:n.-160-67512A=
NM_001128164.1:c.-160-67512A= NP_001121636.1:n.-160-67512A=
NM_001357857.1:c.-189-67512A= NP_001344786.1:n.-189-67512A=
NM_001357857.2:c.-189-67512A= NP_001344786.1:n.-189-67512A=
NM_001128164.2:c.-160-67512A= MANE Select NP_001121636.1:n.-160-67512A=
NM_000332.4:c.-160-67512A= NP_000323.2:n.-160-67512A=