Canonical Allele Identifier: CA1612740173

Gene: ATXN1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.16396038_16396040delinsAAG , CM000668.2:g.16396038_16396040delinsAAG	GRCh38
NC_000006.11:g.16396269_16396271delinsAAG , CM000668.1:g.16396269_16396271delinsAAG	GRCh37
NC_000006.10:g.16504248_16504250delinsAAG	NCBI36
NG_011571.1:g.370451_370453delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436367.6:c.-160-67570_-160-67568delinsCTT MANE Select	ENSP00000416360.1:n.-160-67570_-160-67568delinsCTT
ENST00000244769.8:c.-160-67570_-160-67568delinsCTT	ENSP00000244769.3:n.-160-67570_-160-67568delinsCTT
ENST00000436367.5:c.-160-67570_-160-67568delinsCTT	ENSP00000416360.1:n.-160-67570_-160-67568delinsCTT
NM_000332.3:c.-160-67570_-160-67568delinsCTT	NP_000323.2:n.-160-67570_-160-67568delinsCTT
NM_001128164.1:c.-160-67570_-160-67568delinsCTT	NP_001121636.1:n.-160-67570_-160-67568delinsCTT
NM_001357857.1:c.-189-67570_-189-67568delinsCTT	NP_001344786.1:n.-189-67570_-189-67568delinsCTT
NM_001357857.2:c.-189-67570_-189-67568delinsCTT	NP_001344786.1:n.-189-67570_-189-67568delinsCTT
NM_001128164.2:c.-160-67570_-160-67568delinsCTT MANE Select	NP_001121636.1:n.-160-67570_-160-67568delinsCTT
NM_000332.4:c.-160-67570_-160-67568delinsCTT	NP_000323.2:n.-160-67570_-160-67568delinsCTT