Canonical Allele Identifier: CA1612892811
Gene: ATXN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.16699781C= , CM000668.2:g.16699781C= GRCh38
NC_000006.11:g.16700012C= , CM000668.1:g.16700012C= GRCh37
NC_000006.10:g.16807991C= NCBI36
NG_011571.1:g.66710G=

Transcript Alleles

HGVS Amino-acid change
ENST00000436367.6:c.-614-41880G= MANE Select ENSP00000416360.1:n.-614-41880G=
ENST00000643828.1:n.345-32229G=
ENST00000646259.1:n.189-41880G=
ENST00000675689.1:n.151-41880G=
ENST00000244769.8:c.-614-41880G= ENSP00000244769.3:n.-614-41880G=
ENST00000436367.5:c.-614-41880G= ENSP00000416360.1:n.-614-41880G=
ENST00000473388.6:n.279-41880G=
ENST00000483591.6:n.118-41880G=
ENST00000483954.1:n.160-32229G=
ENST00000495178.1:n.77-41880G=
NM_000332.3:c.-614-41880G= NP_000323.2:n.-614-41880G=
NM_001128164.1:c.-614-41880G= NP_001121636.1:n.-614-41880G=
NM_001357857.1:c.-643-41880G= NP_001344786.1:n.-643-41880G=
NM_001357857.2:c.-643-41880G= NP_001344786.1:n.-643-41880G=
NM_001128164.2:c.-614-41880G= MANE Select NP_001121636.1:n.-614-41880G=
NM_000332.4:c.-614-41880G= NP_000323.2:n.-614-41880G=