Canonical Allele Identifier: CA375323632

Gene: SETX

Linked Data

• dbSNP Id: rs1475374227
• gnomAD v3: 9-132264579-T-C
• gnomAD v4: 9-132264579-T-C
• MyVariant Identifiers: chr9:g.135139966T>C (hg19) ; chr9:g.132264579T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132264579T>C , CM000671.2:g.132264579T>C	GRCh38
NC_000009.11:g.135139966T>C , CM000671.1:g.135139966T>C	GRCh37
NC_000009.10:g.134129787T>C	NCBI36
NG_007946.1:g.95407A>G , LRG_268:g.95407A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000224140.6:c.7694A>G MANE Select	ENSP00000224140.5:p.His2565Arg
ENST00000224140.5:c.7694A>G	ENSP00000224140.5:p.His2565Arg
ENST00000436441.5:c.2507A>G	ENSP00000409143.1:p.His836Arg
ENST00000477049.1:n.844A>G
NM_015046.5:c.7694A>G , LRG_268t1:c.7694A>G	NP_055861.3:p.His2565Arg
XM_005272171.1:c.7781A>G	XP_005272228.1:p.His2594Arg
XM_005272172.1:c.7781A>G	XP_005272229.1:p.His2594Arg
XM_005272173.1:c.7781A>G	XP_005272230.1:p.His2594Arg
XM_011518404.1:c.7781A>G	XP_011516706.1:p.His2594Arg
XM_011518405.1:c.7781A>G	XP_011516707.1:p.His2594Arg
XR_929739.1:n.7610A>G
NM_001351527.1:c.7694A>G	NP_001338456.1:p.His2565Arg
NM_001351528.1:c.7781A>G	NP_001338457.1:p.His2594Arg
NM_015046.6:c.7694A>G	NP_055861.3:p.His2565Arg
XM_005272172.3:c.7781A>G	XP_005272229.1:p.His2594Arg
XM_005272173.3:c.7781A>G	XP_005272230.1:p.His2594Arg
XM_011518404.3:c.7781A>G	XP_011516706.1:p.His2594Arg
XM_011518405.3:c.7781A>G	XP_011516707.1:p.His2594Arg
XM_017014496.1:c.2234A>G	XP_016869985.1:p.His745Arg
XR_001746251.1:n.7249A>G
XR_929739.2:n.7610A>G
NM_015046.7:c.7694A>G MANE Select	NP_055861.3:p.His2565Arg
NM_001351528.2:c.7781A>G	NP_001338457.1:p.His2594Arg
NM_001351527.2:c.7694A>G	NP_001338456.1:p.His2565Arg