Canonical Allele Identifier: CA75749049

Gene: ATXN7

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.63995906C>T , CM000665.2:g.63995906C>T	GRCh38
NC_000003.11:g.63981582C>T , CM000665.1:g.63981582C>T	GRCh37
NC_000003.10:g.63956622C>T	NCBI36
NG_008227.1:g.136350C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000522345.2:c.2084C>T	ENSP00000428067.2:p.Ala695Val
ENST00000674280.1:c.2084C>T MANE Select	ENSP00000501377.1:p.Ala695Val
ENST00000295900.10:c.2084C>T	ENSP00000295900.6:p.Ala695Val
ENST00000474112.5:n.2637C>T
ENST00000484332.1:c.1649C>T	ENSP00000428277.1:p.Ala550Val
ENST00000487717.5:c.2084C>T	ENSP00000420234.1:p.Ala695Val
ENST00000538065.5:c.2084C>T	ENSP00000439585.1:p.Ala695Val
NM_000333.3:c.2084C>T	NP_000324.1:p.Ala695Val
NM_001128149.2:c.1649C>T	NP_001121621.2:p.Ala550Val
NM_001177387.1:c.2084C>T	NP_001170858.1:p.Ala695Val
NM_000333.4:c.2084C>T	NP_000324.1:p.Ala695Val
NM_001128149.3:c.1649C>T	NP_001121621.2:p.Ala550Val
NM_001377405.1:c.2084C>T MANE Select	NP_001364334.1:p.Ala695Val
NM_001377406.1:c.2084C>T	NP_001364335.1:p.Ala695Val