Canonical Allele Identifier: CA375327757

Gene: SETX

Linked Data

• gnomAD v4: 9-132327622-T-C
• MyVariant Identifiers: chr9:g.135203009T>C (hg19) ; chr9:g.132327622T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132327622T>C , CM000671.2:g.132327622T>C	GRCh38
NC_000009.11:g.135203009T>C , CM000671.1:g.135203009T>C	GRCh37
NC_000009.10:g.134192830T>C	NCBI36
NG_007946.1:g.32364A>G , LRG_268:g.32364A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000224140.6:c.3976A>G MANE Select	ENSP00000224140.5:p.Thr1326Ala
ENST00000224140.5:c.3976A>G	ENSP00000224140.5:p.Thr1326Ala
NM_015046.5:c.3976A>G , LRG_268t1:c.3976A>G	NP_055861.3:p.Thr1326Ala
XM_005272171.1:c.3976A>G	XP_005272228.1:p.Thr1326Ala
XM_005272172.1:c.3976A>G	XP_005272229.1:p.Thr1326Ala
XM_005272173.1:c.3976A>G	XP_005272230.1:p.Thr1326Ala
XM_011518404.1:c.3976A>G	XP_011516706.1:p.Thr1326Ala
XM_011518405.1:c.3976A>G	XP_011516707.1:p.Thr1326Ala
XM_011518406.1:c.3976A>G	XP_011516708.1:p.Thr1326Ala
XM_011518407.1:c.3976A>G	XP_011516709.1:p.Thr1326Ala
XM_011518408.1:c.3976A>G	XP_011516710.1:p.Thr1326Ala
XR_929739.1:n.4160A>G
NM_001351527.1:c.3976A>G	NP_001338456.1:p.Thr1326Ala
NM_001351528.1:c.3976A>G	NP_001338457.1:p.Thr1326Ala
NM_015046.6:c.3976A>G	NP_055861.3:p.Thr1326Ala
XM_005272172.3:c.3976A>G	XP_005272229.1:p.Thr1326Ala
XM_005272173.3:c.3976A>G	XP_005272230.1:p.Thr1326Ala
XM_011518404.3:c.3976A>G	XP_011516706.1:p.Thr1326Ala
XM_011518405.3:c.3976A>G	XP_011516707.1:p.Thr1326Ala
XM_011518406.2:c.3976A>G	XP_011516708.1:p.Thr1326Ala
XM_011518408.3:c.3976A>G	XP_011516710.1:p.Thr1326Ala
XR_001746251.1:n.4160A>G
XR_929739.2:n.4160A>G
NM_015046.7:c.3976A>G MANE Select	NP_055861.3:p.Thr1326Ala
NM_001351528.2:c.3976A>G	NP_001338457.1:p.Thr1326Ala
NM_001351527.2:c.3976A>G	NP_001338456.1:p.Thr1326Ala