Canonical Allele Identifier: CA375323609

Gene: SETX

Linked Data

• MyVariant Identifiers: chr9:g.135139963G>T (hg19) ; chr9:g.132264576G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132264576G>T , CM000671.2:g.132264576G>T	GRCh38
NC_000009.11:g.135139963G>T , CM000671.1:g.135139963G>T	GRCh37
NC_000009.10:g.134129784G>T	NCBI36
NG_007946.1:g.95410C>A , LRG_268:g.95410C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224140.6:c.7697C>A MANE Select	ENSP00000224140.5:p.Pro2566His
ENST00000224140.5:c.7697C>A	ENSP00000224140.5:p.Pro2566His
ENST00000436441.5:c.2510C>A	ENSP00000409143.1:p.Pro837His
ENST00000477049.1:n.847C>A
NM_015046.5:c.7697C>A , LRG_268t1:c.7697C>A	NP_055861.3:p.Pro2566His
XM_005272171.1:c.7784C>A	XP_005272228.1:p.Pro2595His
XM_005272172.1:c.7784C>A	XP_005272229.1:p.Pro2595His
XM_005272173.1:c.7784C>A	XP_005272230.1:p.Pro2595His
XM_011518404.1:c.7784C>A	XP_011516706.1:p.Pro2595His
XM_011518405.1:c.7784C>A	XP_011516707.1:p.Pro2595His
XR_929739.1:n.7613C>A
NM_001351527.1:c.7697C>A	NP_001338456.1:p.Pro2566His
NM_001351528.1:c.7784C>A	NP_001338457.1:p.Pro2595His
NM_015046.6:c.7697C>A	NP_055861.3:p.Pro2566His
XM_005272172.3:c.7784C>A	XP_005272229.1:p.Pro2595His
XM_005272173.3:c.7784C>A	XP_005272230.1:p.Pro2595His
XM_011518404.3:c.7784C>A	XP_011516706.1:p.Pro2595His
XM_011518405.3:c.7784C>A	XP_011516707.1:p.Pro2595His
XM_017014496.1:c.2237C>A	XP_016869985.1:p.Pro746His
XR_001746251.1:n.7252C>A
XR_929739.2:n.7613C>A
NM_015046.7:c.7697C>A MANE Select	NP_055861.3:p.Pro2566His
NM_001351528.2:c.7784C>A	NP_001338457.1:p.Pro2595His
NM_001351527.2:c.7697C>A	NP_001338456.1:p.Pro2566His