Canonical Allele Identifier: CA467807443

Gene: SETX

Linked Data

• gnomAD v4: 9-132327620-A-T
• MyVariant Identifiers: chr9:g.135203007A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132327620A>T , CM000671.2:g.132327620A>T	GRCh38
NC_000009.11:g.135203007A>T , CM000671.1:g.135203007A>T	GRCh37
NC_000009.10:g.134192828A>T	NCBI36
NG_007946.1:g.32366T>A , LRG_268:g.32366T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000224140.6:c.3978T>A MANE Select	ENSP00000224140.5:p.Thr1326=
ENST00000224140.5:c.3978T>A	ENSP00000224140.5:p.Thr1326=
NM_015046.5:c.3978T>A , LRG_268t1:c.3978T>A	NP_055861.3:p.Thr1326=
XM_005272171.1:c.3978T>A	XP_005272228.1:p.Thr1326=
XM_005272172.1:c.3978T>A	XP_005272229.1:p.Thr1326=
XM_005272173.1:c.3978T>A	XP_005272230.1:p.Thr1326=
XM_011518404.1:c.3978T>A	XP_011516706.1:p.Thr1326=
XM_011518405.1:c.3978T>A	XP_011516707.1:p.Thr1326=
XM_011518406.1:c.3978T>A	XP_011516708.1:p.Thr1326=
XM_011518407.1:c.3978T>A	XP_011516709.1:p.Thr1326=
XM_011518408.1:c.3978T>A	XP_011516710.1:p.Thr1326=
XR_929739.1:n.4162T>A
NM_001351527.1:c.3978T>A	NP_001338456.1:p.Thr1326=
NM_001351528.1:c.3978T>A	NP_001338457.1:p.Thr1326=
NM_015046.6:c.3978T>A	NP_055861.3:p.Thr1326=
XM_005272172.3:c.3978T>A	XP_005272229.1:p.Thr1326=
XM_005272173.3:c.3978T>A	XP_005272230.1:p.Thr1326=
XM_011518404.3:c.3978T>A	XP_011516706.1:p.Thr1326=
XM_011518405.3:c.3978T>A	XP_011516707.1:p.Thr1326=
XM_011518406.2:c.3978T>A	XP_011516708.1:p.Thr1326=
XM_011518408.3:c.3978T>A	XP_011516710.1:p.Thr1326=
XR_001746251.1:n.4162T>A
XR_929739.2:n.4162T>A
NM_015046.7:c.3978T>A MANE Select	NP_055861.3:p.Thr1326=
NM_001351528.2:c.3978T>A	NP_001338457.1:p.Thr1326=
NM_001351527.2:c.3978T>A	NP_001338456.1:p.Thr1326=