Canonical Allele Identifier: CA5296486

Gene: SETX

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132271714T>C , CM000671.2:g.132271714T>C	GRCh38
NC_000009.11:g.135147101T>C , CM000671.1:g.135147101T>C	GRCh37
NC_000009.10:g.134136922T>C	NCBI36
NG_007946.1:g.88272A>G , LRG_268:g.88272A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_015046.7:c.7195A>G MANE Select	NP_055861.3:p.Ile2399Val
ENST00000224140.6:c.7195A>G MANE Select	ENSP00000224140.5:p.Ile2399Val
NM_001351527.1:c.7195A>G	NP_001338456.1:p.Ile2399Val
NM_001351527.2:c.7195A>G	NP_001338456.1:p.Ile2399Val
NM_001351528.1:c.7195A>G	NP_001338457.1:p.Ile2399Val
NM_001351528.2:c.7195A>G	NP_001338457.1:p.Ile2399Val
NM_015046.5:c.7195A>G , LRG_268t1:c.7195A>G	NP_055861.3:p.Ile2399Val
NM_015046.6:c.7195A>G	NP_055861.3:p.Ile2399Val
ENST00000224140.5:c.7195A>G	ENSP00000224140.5:p.Ile2399Val
ENST00000436441.5:c.1921A>G	ENSP00000409143.1:p.Ile641Val
ENST00000477049.1:n.222A>G
XM_005272171.1:c.7195A>G	XP_005272228.1:p.Ile2399Val
XM_005272172.1:c.7195A>G	XP_005272229.1:p.Ile2399Val
XM_005272172.3:c.7195A>G	XP_005272229.1:p.Ile2399Val
XM_005272173.1:c.7195A>G	XP_005272230.1:p.Ile2399Val
XM_005272173.3:c.7195A>G	XP_005272230.1:p.Ile2399Val
XM_011518404.1:c.7195A>G	XP_011516706.1:p.Ile2399Val
XM_011518404.3:c.7195A>G	XP_011516706.1:p.Ile2399Val
XM_011518405.1:c.7195A>G	XP_011516707.1:p.Ile2399Val
XM_011518405.3:c.7195A>G	XP_011516707.1:p.Ile2399Val
XM_011518406.1:c.7195A>G	XP_011516708.1:p.Ile2399Val
XM_011518406.2:c.7195A>G	XP_011516708.1:p.Ile2399Val
XM_017014496.1:c.1648A>G	XP_016869985.1:p.Ile550Val
XR_001746251.1:n.6750A>G
XR_929739.1:n.7111A>G
XR_929739.2:n.7111A>G