Canonical Allele Identifier: CA16043862
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 374712
ClinVar RCV Id: RCV000415862
dbSNP Id: rs1057519213

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.132275315dup , CM000671.2:g.132275315dup GRCh38
NC_000009.11:g.135150702dup , CM000671.1:g.135150702dup GRCh37
NC_000009.10:g.134140523dup NCBI36
NG_007946.1:g.84672dup , LRG_268:g.84672dup

Transcript Alleles

HGVS Amino-acid change
ENST00000224140.6:c.7042dup MANE Select ENSP00000224140.5:p.Tyr2348LeufsTer18
ENST00000224140.5:c.7042dup ENSP00000224140.5:p.Tyr2348LeufsTer18
ENST00000436441.5:c.1768dup ENSP00000409143.1:p.Tyr590LeufsTer18
ENST00000464133.1:n.240dup
ENST00000477049.1:n.69dup
NM_015046.5:c.7042dup , LRG_268t1:c.7042dup NP_055861.3:p.Tyr2348LeufsTer18
XM_005272171.1:c.7042dup XP_005272228.1:p.Tyr2348LeufsTer18
XM_005272172.1:c.7042dup XP_005272229.1:p.Tyr2348LeufsTer18
XM_005272173.1:c.7042dup XP_005272230.1:p.Tyr2348LeufsTer18
XM_011518404.1:c.7042dup XP_011516706.1:p.Tyr2348LeufsTer18
XM_011518405.1:c.7042dup XP_011516707.1:p.Tyr2348LeufsTer18
XM_011518406.1:c.7042dup XP_011516708.1:p.Tyr2348LeufsTer18
XM_011518407.1:c.7042dup XP_011516709.1:p.Tyr2348LeufsTer18
XR_929739.1:n.6958dup
NM_001351527.1:c.7042dup NP_001338456.1:p.Tyr2348LeufsTer18
NM_001351528.1:c.7042dup NP_001338457.1:p.Tyr2348LeufsTer18
NM_015046.6:c.7042dup NP_055861.3:p.Tyr2348LeufsTer18
XM_005272172.3:c.7042dup XP_005272229.1:p.Tyr2348LeufsTer18
XM_005272173.3:c.7042dup XP_005272230.1:p.Tyr2348LeufsTer18
XM_011518404.3:c.7042dup XP_011516706.1:p.Tyr2348LeufsTer18
XM_011518405.3:c.7042dup XP_011516707.1:p.Tyr2348LeufsTer18
XM_011518406.2:c.7042dup XP_011516708.1:p.Tyr2348LeufsTer18
XM_017014496.1:c.1495dup XP_016869985.1:p.Tyr499LeufsTer18
XR_001746251.1:n.6597dup
XR_929739.2:n.6958dup
NM_015046.7:c.7042dup MANE Select NP_055861.3:p.Tyr2348LeufsTer18
NM_001351528.2:c.7042dup NP_001338457.1:p.Tyr2348LeufsTer18
NM_001351527.2:c.7042dup NP_001338456.1:p.Tyr2348LeufsTer18