Canonical Allele Identifier: CA1882150120
Gene: SETX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.132329796G= , CM000671.2:g.132329796G= GRCh38
NC_000009.11:g.135205183G= , CM000671.1:g.135205183G= GRCh37
NC_000009.10:g.134195004G= NCBI36
NG_007946.1:g.30190C= , LRG_268:g.30190C=

Transcript Alleles

HGVS Amino-acid change
ENST00000224140.6:c.1802C= MANE Select ENSP00000224140.5:p.Pro601=
ENST00000224140.5:c.1802C= ENSP00000224140.5:p.Pro601=
NM_015046.5:c.1802C= , LRG_268t1:c.1802C= NP_055861.3:p.Pro601=
XM_005272171.1:c.1802C= XP_005272228.1:p.Pro601=
XM_005272172.1:c.1802C= XP_005272229.1:p.Pro601=
XM_005272173.1:c.1802C= XP_005272230.1:p.Pro601=
XM_011518404.1:c.1802C= XP_011516706.1:p.Pro601=
XM_011518405.1:c.1802C= XP_011516707.1:p.Pro601=
XM_011518406.1:c.1802C= XP_011516708.1:p.Pro601=
XM_011518407.1:c.1802C= XP_011516709.1:p.Pro601=
XM_011518408.1:c.1802C= XP_011516710.1:p.Pro601=
XR_929739.1:n.1986C=
NM_001351527.1:c.1802C= NP_001338456.1:p.Pro601=
NM_001351528.1:c.1802C= NP_001338457.1:p.Pro601=
NM_015046.6:c.1802C= NP_055861.3:p.Pro601=
XM_005272172.3:c.1802C= XP_005272229.1:p.Pro601=
XM_005272173.3:c.1802C= XP_005272230.1:p.Pro601=
XM_011518404.3:c.1802C= XP_011516706.1:p.Pro601=
XM_011518405.3:c.1802C= XP_011516707.1:p.Pro601=
XM_011518406.2:c.1802C= XP_011516708.1:p.Pro601=
XM_011518408.3:c.1802C= XP_011516710.1:p.Pro601=
XR_001746251.1:n.1986C=
XR_929739.2:n.1986C=
NM_015046.7:c.1802C= MANE Select NP_055861.3:p.Pro601=
NM_001351528.2:c.1802C= NP_001338457.1:p.Pro601=
NM_001351527.2:c.1802C= NP_001338456.1:p.Pro601=