Canonical Allele Identifier: CA1129647069

Gene: SETX

Linked Data

• dbSNP Id: rs1465985294
• gnomAD v3: 9-132296765-TAAAA-T
• gnomAD v4: 9-132296765-TAAAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132296768_132296771del , CM000671.2:g.132296768_132296771del	GRCh38
NC_000009.11:g.135172155_135172158del , CM000671.1:g.135172155_135172158del	GRCh37
NC_000009.10:g.134161976_134161979del	NCBI36
NG_007946.1:g.63217_63220del , LRG_268:g.63217_63220del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224140.6:c.5949+118_5949+121del MANE Select	ENSP00000224140.5:n.5949+118_5949+121del
ENST00000224140.5:c.5949+118_5949+121del	ENSP00000224140.5:n.5949+118_5949+121del
ENST00000436441.5:c.675+118_675+121del	ENSP00000409143.1:n.675+118_675+121del
NM_015046.5:c.5949+118_5949+121del , LRG_268t1:c.5949+118_5949+121del	NP_055861.3:n.5949+118_5949+121del
XM_005272171.1:c.5949+118_5949+121del	XP_005272228.1:n.5949+118_5949+121del
XM_005272172.1:c.5949+118_5949+121del	XP_005272229.1:n.5949+118_5949+121del
XM_005272173.1:c.5949+118_5949+121del	XP_005272230.1:n.5949+118_5949+121del
XM_011518404.1:c.5949+118_5949+121del	XP_011516706.1:n.5949+118_5949+121del
XM_011518405.1:c.5949+118_5949+121del	XP_011516707.1:n.5949+118_5949+121del
XM_011518406.1:c.5949+118_5949+121del	XP_011516708.1:n.5949+118_5949+121del
XM_011518407.1:c.5949+118_5949+121del	XP_011516709.1:n.5949+118_5949+121del
XM_011518408.1:c.5949+118_5949+121del	XP_011516710.1:n.5949+118_5949+121del
XR_929739.1:n.5865+118_5865+121del
NM_001351527.1:c.5949+118_5949+121del	NP_001338456.1:n.5949+118_5949+121del
NM_001351528.1:c.5949+118_5949+121del	NP_001338457.1:n.5949+118_5949+121del
NM_015046.6:c.5949+118_5949+121del	NP_055861.3:n.5949+118_5949+121del
XM_005272172.3:c.5949+118_5949+121del	XP_005272229.1:n.5949+118_5949+121del
XM_005272173.3:c.5949+118_5949+121del	XP_005272230.1:n.5949+118_5949+121del
XM_011518404.3:c.5949+118_5949+121del	XP_011516706.1:n.5949+118_5949+121del
XM_011518405.3:c.5949+118_5949+121del	XP_011516707.1:n.5949+118_5949+121del
XM_011518406.2:c.5949+118_5949+121del	XP_011516708.1:n.5949+118_5949+121del
XM_011518408.3:c.5949+118_5949+121del	XP_011516710.1:n.5949+118_5949+121del
XM_017014496.1:c.402+118_402+121del	XP_016869985.1:n.402+118_402+121del
XR_001746251.1:n.5504+118_5504+121del
XR_929739.2:n.5865+118_5865+121del
NM_015046.7:c.5949+118_5949+121del MANE Select	NP_055861.3:n.5949+118_5949+121del
NM_001351528.2:c.5949+118_5949+121del	NP_001338457.1:n.5949+118_5949+121del
NM_001351527.2:c.5949+118_5949+121del	NP_001338456.1:n.5949+118_5949+121del