Canonical Allele Identifier: CA7314309

Gene: TRIP11 ATXN3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92039611G>A , CM000676.2:g.92039611G>A	GRCh38
NC_000014.8:g.92505955G>A , CM000676.1:g.92505955G>A	GRCh37
NC_000014.7:g.91575708G>A	NCBI36
NG_008198.2:g.72011C>T
NG_016970.1:g.5449C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267622.8:c.75C>T (TRIP11) MANE Select	ENSP00000267622.4:p.Ser25=
ENST00000555105.1:n.407C>T (TRIP11)
ENST00000555516.6:c.-345+1269C>T (TRIP11)	ENSP00000451944.1:n.-345+1269C>T
ENST00000558190.5:c.*24709C>T (ATXN3)	ENSP00000478320.1:n.*24709C>T
NM_004239.3:c.75C>T (TRIP11)	NP_004230.2:p.Ser25=
XM_005268215.2:c.75C>T (TRIP11)	XP_005268272.1:p.Ser25=
XM_006720321.2:c.75C>T (TRIP11)	XP_006720384.1:p.Ser25=
XM_011537361.1:c.75C>T (TRIP11)	XP_011535663.1:p.Ser25=
XR_943560.1:n.530C>T (TRIP11)
NM_001321851.1:c.75C>T (TRIP11)	NP_001308780.1:p.Ser25=
NM_004239.4:c.75C>T (TRIP11) MANE Select	NP_004230.2:p.Ser25=
XM_017021787.2:c.-672C>T (TRIP11)	XP_016877276.1:n.-672C>T
XM_017021788.2:c.-1124C>T (TRIP11)	XP_016877277.1:n.-1124C>T
XR_001750598.2:n.524C>T (TRIP11)
XR_943560.2:n.524C>T (TRIP11)