Canonical Allele Identifier: CA5297105

Gene: SETX

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132326667A>G , CM000671.2:g.132326667A>G	GRCh38
NC_000009.11:g.135202054A>G , CM000671.1:g.135202054A>G	GRCh37
NC_000009.10:g.134191875A>G	NCBI36
NG_007946.1:g.33319T>C , LRG_268:g.33319T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_015046.7:c.4931T>C MANE Select	NP_055861.3:p.Ile1644Thr
ENST00000224140.6:c.4931T>C MANE Select	ENSP00000224140.5:p.Ile1644Thr
NM_001351527.1:c.4931T>C	NP_001338456.1:p.Ile1644Thr
NM_001351527.2:c.4931T>C	NP_001338456.1:p.Ile1644Thr
NM_001351528.1:c.4931T>C	NP_001338457.1:p.Ile1644Thr
NM_001351528.2:c.4931T>C	NP_001338457.1:p.Ile1644Thr
NM_015046.5:c.4931T>C , LRG_268t1:c.4931T>C	NP_055861.3:p.Ile1644Thr
NM_015046.6:c.4931T>C	NP_055861.3:p.Ile1644Thr
ENST00000224140.5:c.4931T>C	ENSP00000224140.5:p.Ile1644Thr
XM_005272171.1:c.4931T>C	XP_005272228.1:p.Ile1644Thr
XM_005272172.1:c.4931T>C	XP_005272229.1:p.Ile1644Thr
XM_005272172.3:c.4931T>C	XP_005272229.1:p.Ile1644Thr
XM_005272173.1:c.4931T>C	XP_005272230.1:p.Ile1644Thr
XM_005272173.3:c.4931T>C	XP_005272230.1:p.Ile1644Thr
XM_011518404.1:c.4931T>C	XP_011516706.1:p.Ile1644Thr
XM_011518404.3:c.4931T>C	XP_011516706.1:p.Ile1644Thr
XM_011518405.1:c.4931T>C	XP_011516707.1:p.Ile1644Thr
XM_011518405.3:c.4931T>C	XP_011516707.1:p.Ile1644Thr
XM_011518406.1:c.4931T>C	XP_011516708.1:p.Ile1644Thr
XM_011518406.2:c.4931T>C	XP_011516708.1:p.Ile1644Thr
XM_011518407.1:c.4931T>C	XP_011516709.1:p.Ile1644Thr
XM_011518408.1:c.4931T>C	XP_011516710.1:p.Ile1644Thr
XM_011518408.3:c.4931T>C	XP_011516710.1:p.Ile1644Thr
XM_017014496.1:c.-274+286T>C	XP_016869985.1:n.-274+286T>C
XR_001746251.1:n.4829+286T>C
XR_929739.1:n.5115T>C
XR_929739.2:n.5115T>C