Canonical Allele Identifier: CA1612892796
Gene: ATXN1 HGNC NCBI

Linked Data

dbSNP Id: rs570943684

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.16699763A>C , CM000668.2:g.16699763A>C GRCh38
NC_000006.11:g.16699994A>C , CM000668.1:g.16699994A>C GRCh37
NC_000006.10:g.16807973A>C NCBI36
NG_011571.1:g.66728T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000436367.6:c.-614-41862T>G MANE Select ENSP00000416360.1:n.-614-41862T>G
ENST00000643828.1:n.345-32211T>G
ENST00000646259.1:n.189-41862T>G
ENST00000675689.1:n.151-41862T>G
ENST00000244769.8:c.-614-41862T>G ENSP00000244769.3:n.-614-41862T>G
ENST00000436367.5:c.-614-41862T>G ENSP00000416360.1:n.-614-41862T>G
ENST00000473388.6:n.279-41862T>G
ENST00000483591.6:n.118-41862T>G
ENST00000483954.1:n.160-32211T>G
ENST00000495178.1:n.77-41862T>G
NM_000332.3:c.-614-41862T>G NP_000323.2:n.-614-41862T>G
NM_001128164.1:c.-614-41862T>G NP_001121636.1:n.-614-41862T>G
NM_001357857.1:c.-643-41862T>G NP_001344786.1:n.-643-41862T>G
NM_001357857.2:c.-643-41862T>G NP_001344786.1:n.-643-41862T>G
NM_001128164.2:c.-614-41862T>G MANE Select NP_001121636.1:n.-614-41862T>G
NM_000332.4:c.-614-41862T>G NP_000323.2:n.-614-41862T>G