Canonical Allele Identifier: CA375323521

Gene: SETX

Linked Data

• MyVariant Identifiers: chr9:g.135139952G>C (hg19) ; chr9:g.132264565G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132264565G>C , CM000671.2:g.132264565G>C	GRCh38
NC_000009.11:g.135139952G>C , CM000671.1:g.135139952G>C	GRCh37
NC_000009.10:g.134129773G>C	NCBI36
NG_007946.1:g.95421C>G , LRG_268:g.95421C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224140.6:c.7708C>G MANE Select	ENSP00000224140.5:p.Pro2570Ala
ENST00000224140.5:c.7708C>G	ENSP00000224140.5:p.Pro2570Ala
ENST00000436441.5:c.2521C>G	ENSP00000409143.1:p.Pro841Ala
ENST00000477049.1:n.858C>G
NM_015046.5:c.7708C>G , LRG_268t1:c.7708C>G	NP_055861.3:p.Pro2570Ala
XM_005272171.1:c.7795C>G	XP_005272228.1:p.Pro2599Ala
XM_005272172.1:c.7795C>G	XP_005272229.1:p.Pro2599Ala
XM_005272173.1:c.7795C>G	XP_005272230.1:p.Pro2599Ala
XM_011518404.1:c.7795C>G	XP_011516706.1:p.Pro2599Ala
XM_011518405.1:c.7795C>G	XP_011516707.1:p.Pro2599Ala
XR_929739.1:n.7624C>G
NM_001351527.1:c.7708C>G	NP_001338456.1:p.Pro2570Ala
NM_001351528.1:c.7795C>G	NP_001338457.1:p.Pro2599Ala
NM_015046.6:c.7708C>G	NP_055861.3:p.Pro2570Ala
XM_005272172.3:c.7795C>G	XP_005272229.1:p.Pro2599Ala
XM_005272173.3:c.7795C>G	XP_005272230.1:p.Pro2599Ala
XM_011518404.3:c.7795C>G	XP_011516706.1:p.Pro2599Ala
XM_011518405.3:c.7795C>G	XP_011516707.1:p.Pro2599Ala
XM_017014496.1:c.2248C>G	XP_016869985.1:p.Pro750Ala
XR_001746251.1:n.7263C>G
XR_929739.2:n.7624C>G
NM_015046.7:c.7708C>G MANE Select	NP_055861.3:p.Pro2570Ala
NM_001351528.2:c.7795C>G	NP_001338457.1:p.Pro2599Ala
NM_001351527.2:c.7708C>G	NP_001338456.1:p.Pro2570Ala