Canonical Allele Identifier: CA1612873025

Gene: ATXN1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.16741849C= , CM000668.2:g.16741849C=	GRCh38
NC_000006.11:g.16742080C= , CM000668.1:g.16742080C=	GRCh37
NC_000006.10:g.16850059C=	NCBI36
NG_011571.1:g.24642G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000436367.6:c.-615+11384G= MANE Select	ENSP00000416360.1:n.-615+11384G=
ENST00000643828.1:n.344+11384G=
ENST00000646259.1:n.188+11384G=
ENST00000675689.1:n.150+11384G=
ENST00000676138.1:n.162-1931G=
ENST00000244769.8:c.-615+11384G=	ENSP00000244769.3:n.-615+11384G=
ENST00000436367.5:c.-615+11384G=	ENSP00000416360.1:n.-615+11384G=
ENST00000467008.5:n.295-1931G=
ENST00000473388.6:n.278+11384G=
ENST00000483591.6:n.117+8127G=
ENST00000483954.1:n.159+19449G=
ENST00000492857.1:n.331-1931G=
ENST00000495178.1:n.76+11384G=
ENST00000498374.1:n.195-1931G=
NM_000332.3:c.-615+11384G=	NP_000323.2:n.-615+11384G=
NM_001128164.1:c.-615+11384G=	NP_001121636.1:n.-615+11384G=
NM_001357857.1:c.-644+11384G=	NP_001344786.1:n.-644+11384G=
NR_152111.1:n.309-1931G=
NR_152112.1:n.194-1931G=
NR_152113.1:n.191-1931G=
NR_152114.1:n.240-1931G=
NM_001357857.2:c.-644+11384G=	NP_001344786.1:n.-644+11384G=
NR_152111.2:n.279-1931G=
NR_152112.2:n.164-1931G=
NR_152113.2:n.244-1931G=
NR_152114.2:n.293-1931G=
NM_001128164.2:c.-615+11384G= MANE Select	NP_001121636.1:n.-615+11384G=
NR_152111.3:n.279-1931G=
NR_152112.3:n.164-1931G=
NR_152113.3:n.244-1931G=
NR_152114.3:n.293-1931G=
NM_000332.4:c.-615+11384G=	NP_000323.2:n.-615+11384G=