Canonical Allele Identifier: CA375323562

Gene: SETX

Linked Data

• MyVariant Identifiers: chr9:g.135139958C>T (hg19) ; chr9:g.132264571C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132264571C>T , CM000671.2:g.132264571C>T	GRCh38
NC_000009.11:g.135139958C>T , CM000671.1:g.135139958C>T	GRCh37
NC_000009.10:g.134129779C>T	NCBI36
NG_007946.1:g.95415G>A , LRG_268:g.95415G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000224140.6:c.7702G>A MANE Select	ENSP00000224140.5:p.Ala2568Thr
ENST00000224140.5:c.7702G>A	ENSP00000224140.5:p.Ala2568Thr
ENST00000436441.5:c.2515G>A	ENSP00000409143.1:p.Ala839Thr
ENST00000477049.1:n.852G>A
NM_015046.5:c.7702G>A , LRG_268t1:c.7702G>A	NP_055861.3:p.Ala2568Thr
XM_005272171.1:c.7789G>A	XP_005272228.1:p.Ala2597Thr
XM_005272172.1:c.7789G>A	XP_005272229.1:p.Ala2597Thr
XM_005272173.1:c.7789G>A	XP_005272230.1:p.Ala2597Thr
XM_011518404.1:c.7789G>A	XP_011516706.1:p.Ala2597Thr
XM_011518405.1:c.7789G>A	XP_011516707.1:p.Ala2597Thr
XR_929739.1:n.7618G>A
NM_001351527.1:c.7702G>A	NP_001338456.1:p.Ala2568Thr
NM_001351528.1:c.7789G>A	NP_001338457.1:p.Ala2597Thr
NM_015046.6:c.7702G>A	NP_055861.3:p.Ala2568Thr
XM_005272172.3:c.7789G>A	XP_005272229.1:p.Ala2597Thr
XM_005272173.3:c.7789G>A	XP_005272230.1:p.Ala2597Thr
XM_011518404.3:c.7789G>A	XP_011516706.1:p.Ala2597Thr
XM_011518405.3:c.7789G>A	XP_011516707.1:p.Ala2597Thr
XM_017014496.1:c.2242G>A	XP_016869985.1:p.Ala748Thr
XR_001746251.1:n.7257G>A
XR_929739.2:n.7618G>A
NM_015046.7:c.7702G>A MANE Select	NP_055861.3:p.Ala2568Thr
NM_001351528.2:c.7789G>A	NP_001338457.1:p.Ala2597Thr
NM_001351527.2:c.7702G>A	NP_001338456.1:p.Ala2568Thr