Canonical Allele Identifier: CA467504616

Gene: SETX

Linked Data

• MyVariant Identifiers: chr9:g.135139956T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132264569T>G , CM000671.2:g.132264569T>G	GRCh38
NC_000009.11:g.135139956T>G , CM000671.1:g.135139956T>G	GRCh37
NC_000009.10:g.134129777T>G	NCBI36
NG_007946.1:g.95417A>C , LRG_268:g.95417A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224140.6:c.7704A>C MANE Select	ENSP00000224140.5:p.Ala2568=
ENST00000224140.5:c.7704A>C	ENSP00000224140.5:p.Ala2568=
ENST00000436441.5:c.2517A>C	ENSP00000409143.1:p.Ala839=
ENST00000477049.1:n.854A>C
NM_015046.5:c.7704A>C , LRG_268t1:c.7704A>C	NP_055861.3:p.Ala2568=
XM_005272171.1:c.7791A>C	XP_005272228.1:p.Ala2597=
XM_005272172.1:c.7791A>C	XP_005272229.1:p.Ala2597=
XM_005272173.1:c.7791A>C	XP_005272230.1:p.Ala2597=
XM_011518404.1:c.7791A>C	XP_011516706.1:p.Ala2597=
XM_011518405.1:c.7791A>C	XP_011516707.1:p.Ala2597=
XR_929739.1:n.7620A>C
NM_001351527.1:c.7704A>C	NP_001338456.1:p.Ala2568=
NM_001351528.1:c.7791A>C	NP_001338457.1:p.Ala2597=
NM_015046.6:c.7704A>C	NP_055861.3:p.Ala2568=
XM_005272172.3:c.7791A>C	XP_005272229.1:p.Ala2597=
XM_005272173.3:c.7791A>C	XP_005272230.1:p.Ala2597=
XM_011518404.3:c.7791A>C	XP_011516706.1:p.Ala2597=
XM_011518405.3:c.7791A>C	XP_011516707.1:p.Ala2597=
XM_017014496.1:c.2244A>C	XP_016869985.1:p.Ala748=
XR_001746251.1:n.7259A>C
XR_929739.2:n.7620A>C
NM_015046.7:c.7704A>C MANE Select	NP_055861.3:p.Ala2568=
NM_001351528.2:c.7791A>C	NP_001338457.1:p.Ala2597=
NM_001351527.2:c.7704A>C	NP_001338456.1:p.Ala2568=