Canonical Allele Identifier: CA565761802

Gene: ATXN1

Linked Data

• dbSNP Id: rs1326664655
• gnomAD v2: 6-16699968-T-C
• gnomAD v3: 6-16699737-T-C
• gnomAD v4: 6-16699737-T-C
• MyVariant Identifiers: chr6:g.16699968T>C (hg19) ; chr6:g.16699737T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.16699737T>C , CM000668.2:g.16699737T>C	GRCh38
NC_000006.11:g.16699968T>C , CM000668.1:g.16699968T>C	GRCh37
NC_000006.10:g.16807947T>C	NCBI36
NG_011571.1:g.66754A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000436367.6:c.-614-41836A>G MANE Select	ENSP00000416360.1:n.-614-41836A>G
ENST00000643828.1:n.345-32185A>G
ENST00000646259.1:n.189-41836A>G
ENST00000675689.1:n.151-41836A>G
ENST00000244769.8:c.-614-41836A>G	ENSP00000244769.3:n.-614-41836A>G
ENST00000436367.5:c.-614-41836A>G	ENSP00000416360.1:n.-614-41836A>G
ENST00000473388.6:n.279-41836A>G
ENST00000483591.6:n.118-41836A>G
ENST00000483954.1:n.160-32185A>G
ENST00000495178.1:n.77-41836A>G
NM_000332.3:c.-614-41836A>G	NP_000323.2:n.-614-41836A>G
NM_001128164.1:c.-614-41836A>G	NP_001121636.1:n.-614-41836A>G
NM_001357857.1:c.-643-41836A>G	NP_001344786.1:n.-643-41836A>G
NM_001357857.2:c.-643-41836A>G	NP_001344786.1:n.-643-41836A>G
NM_001128164.2:c.-614-41836A>G MANE Select	NP_001121636.1:n.-614-41836A>G
NM_000332.4:c.-614-41836A>G	NP_000323.2:n.-614-41836A>G