Canonical Allele Identifier: CA5296530

Gene: SETX

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132275298G>A , CM000671.2:g.132275298G>A	GRCh38
NC_000009.11:g.135150685G>A , CM000671.1:g.135150685G>A	GRCh37
NC_000009.10:g.134140506G>A	NCBI36
NG_007946.1:g.84688C>T , LRG_268:g.84688C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_015046.7:c.7058C>T MANE Select	NP_055861.3:p.Thr2353Met
ENST00000224140.6:c.7058C>T MANE Select	ENSP00000224140.5:p.Thr2353Met
NM_001351527.1:c.7058C>T	NP_001338456.1:p.Thr2353Met
NM_001351527.2:c.7058C>T	NP_001338456.1:p.Thr2353Met
NM_001351528.1:c.7058C>T	NP_001338457.1:p.Thr2353Met
NM_001351528.2:c.7058C>T	NP_001338457.1:p.Thr2353Met
NM_015046.5:c.7058C>T , LRG_268t1:c.7058C>T	NP_055861.3:p.Thr2353Met
NM_015046.6:c.7058C>T	NP_055861.3:p.Thr2353Met
ENST00000224140.5:c.7058C>T	ENSP00000224140.5:p.Thr2353Met
ENST00000436441.5:c.1784C>T	ENSP00000409143.1:p.Thr595Met
ENST00000464133.1:n.256C>T
ENST00000477049.1:n.85C>T
XM_005272171.1:c.7058C>T	XP_005272228.1:p.Thr2353Met
XM_005272172.1:c.7058C>T	XP_005272229.1:p.Thr2353Met
XM_005272172.3:c.7058C>T	XP_005272229.1:p.Thr2353Met
XM_005272173.1:c.7058C>T	XP_005272230.1:p.Thr2353Met
XM_005272173.3:c.7058C>T	XP_005272230.1:p.Thr2353Met
XM_011518404.1:c.7058C>T	XP_011516706.1:p.Thr2353Met
XM_011518404.3:c.7058C>T	XP_011516706.1:p.Thr2353Met
XM_011518405.1:c.7058C>T	XP_011516707.1:p.Thr2353Met
XM_011518405.3:c.7058C>T	XP_011516707.1:p.Thr2353Met
XM_011518406.1:c.7058C>T	XP_011516708.1:p.Thr2353Met
XM_011518406.2:c.7058C>T	XP_011516708.1:p.Thr2353Met
XM_011518407.1:c.7058C>T	XP_011516709.1:p.Thr2353Met
XM_017014496.1:c.1511C>T	XP_016869985.1:p.Thr504Met
XR_001746251.1:n.6613C>T
XR_929739.1:n.6974C>T
XR_929739.2:n.6974C>T