Canonical Allele Identifier: CA5296357
Community Standard Title: NM_015046.7(SETX):c.7682C>T (p.Ser2561Leu)
Gene: SETX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.132264591G>A , CM000671.2:g.132264591G>A GRCh38
NC_000009.11:g.135139978G>A , CM000671.1:g.135139978G>A GRCh37
NC_000009.10:g.134129799G>A NCBI36
NG_007946.1:g.95395C>T , LRG_268:g.95395C>T

Transcript Alleles

HGVS Amino-acid Change
NM_015046.7:c.7682C>T MANE Select NP_055861.3:p.Ser2561Leu
ENST00000224140.6:c.7682C>T MANE Select ENSP00000224140.5:p.Ser2561Leu
NM_001351527.1:c.7682C>T NP_001338456.1:p.Ser2561Leu
NM_001351527.2:c.7682C>T NP_001338456.1:p.Ser2561Leu
NM_001351528.1:c.7769C>T NP_001338457.1:p.Ser2590Leu
NM_001351528.2:c.7769C>T NP_001338457.1:p.Ser2590Leu
NM_015046.5:c.7682C>T , LRG_268t1:c.7682C>T NP_055861.3:p.Ser2561Leu
NM_015046.6:c.7682C>T NP_055861.3:p.Ser2561Leu
ENST00000224140.5:c.7682C>T ENSP00000224140.5:p.Ser2561Leu
ENST00000436441.5:c.2495C>T ENSP00000409143.1:p.Ser832Leu
ENST00000477049.1:n.832C>T
XM_005272171.1:c.7769C>T XP_005272228.1:p.Ser2590Leu
XM_005272172.1:c.7769C>T XP_005272229.1:p.Ser2590Leu
XM_005272172.3:c.7769C>T XP_005272229.1:p.Ser2590Leu
XM_005272173.1:c.7769C>T XP_005272230.1:p.Ser2590Leu
XM_005272173.3:c.7769C>T XP_005272230.1:p.Ser2590Leu
XM_011518404.1:c.7769C>T XP_011516706.1:p.Ser2590Leu
XM_011518404.3:c.7769C>T XP_011516706.1:p.Ser2590Leu
XM_011518405.1:c.7769C>T XP_011516707.1:p.Ser2590Leu
XM_011518405.3:c.7769C>T XP_011516707.1:p.Ser2590Leu
XM_017014496.1:c.2222C>T XP_016869985.1:p.Ser741Leu
XR_001746251.1:n.7237C>T
XR_929739.1:n.7598C>T
XR_929739.2:n.7598C>T