Canonical Allele Identifier: CA467504631

Gene: SETX

Linked Data

• MyVariant Identifiers: chr9:g.135139962A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132264575A>C , CM000671.2:g.132264575A>C	GRCh38
NC_000009.11:g.135139962A>C , CM000671.1:g.135139962A>C	GRCh37
NC_000009.10:g.134129783A>C	NCBI36
NG_007946.1:g.95411T>G , LRG_268:g.95411T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000224140.6:c.7698T>G MANE Select	ENSP00000224140.5:p.Pro2566=
ENST00000224140.5:c.7698T>G	ENSP00000224140.5:p.Pro2566=
ENST00000436441.5:c.2511T>G	ENSP00000409143.1:p.Pro837=
ENST00000477049.1:n.848T>G
NM_015046.5:c.7698T>G , LRG_268t1:c.7698T>G	NP_055861.3:p.Pro2566=
XM_005272171.1:c.7785T>G	XP_005272228.1:p.Pro2595=
XM_005272172.1:c.7785T>G	XP_005272229.1:p.Pro2595=
XM_005272173.1:c.7785T>G	XP_005272230.1:p.Pro2595=
XM_011518404.1:c.7785T>G	XP_011516706.1:p.Pro2595=
XM_011518405.1:c.7785T>G	XP_011516707.1:p.Pro2595=
XR_929739.1:n.7614T>G
NM_001351527.1:c.7698T>G	NP_001338456.1:p.Pro2566=
NM_001351528.1:c.7785T>G	NP_001338457.1:p.Pro2595=
NM_015046.6:c.7698T>G	NP_055861.3:p.Pro2566=
XM_005272172.3:c.7785T>G	XP_005272229.1:p.Pro2595=
XM_005272173.3:c.7785T>G	XP_005272230.1:p.Pro2595=
XM_011518404.3:c.7785T>G	XP_011516706.1:p.Pro2595=
XM_011518405.3:c.7785T>G	XP_011516707.1:p.Pro2595=
XM_017014496.1:c.2238T>G	XP_016869985.1:p.Pro746=
XR_001746251.1:n.7253T>G
XR_929739.2:n.7614T>G
NM_015046.7:c.7698T>G MANE Select	NP_055861.3:p.Pro2566=
NM_001351528.2:c.7785T>G	NP_001338457.1:p.Pro2595=
NM_001351527.2:c.7698T>G	NP_001338456.1:p.Pro2566=