Canonical Allele Identifier: CA2773388372
Gene: STX11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.144186912_144186922del , CM000668.2:g.144186912_144186922del GRCh38
NC_000006.11:g.144508049_144508059del , CM000668.1:g.144508049_144508059del GRCh37
NC_000006.10:g.144549742_144549752del NCBI36
NG_007613.1:g.41396_41406del , LRG_113:g.41396_41406del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698355.1:c.285_295del ENSP00000513678.1:p.Arg96HisfsTer16
ENST00000698356.1:c.285_295del ENSP00000513679.1:p.Arg96HisfsTer16
ENST00000698357.1:c.285_295del ENSP00000513680.1:p.Arg96HisfsTer16
ENST00000367568.5:c.285_295del MANE Select ENSP00000356540.4:p.Arg96HisfsTer16
ENST00000367568.4:c.285_295del ENSP00000356540.4:p.Arg96HisfsTer16
NM_003764.3:c.285_295del , LRG_113t1:c.285_295del NP_003755.2:p.Arg96HisfsTer16
XM_011536213.1:c.363_373del XP_011534515.1:p.Arg122HisfsTer16
XM_011536214.1:c.285_295del XP_011534516.1:p.Arg96HisfsTer16
XM_011536215.1:c.285_295del XP_011534517.1:p.Arg96HisfsTer16
XM_011536216.1:c.285_295del XP_011534518.1:p.Arg96HisfsTer16
XM_011536217.1:c.285_295del XP_011534519.1:p.Arg96HisfsTer16
XM_011536218.1:c.285_295del XP_011534520.1:p.Arg96HisfsTer16
XM_011536213.2:c.363_373del XP_011534515.1:p.Arg122HisfsTer16
XM_011536214.2:c.285_295del XP_011534516.1:p.Arg96HisfsTer16
XM_011536217.2:c.285_295del XP_011534519.1:p.Arg96HisfsTer16
XM_011536218.2:c.285_295del XP_011534520.1:p.Arg96HisfsTer16
XM_017011400.1:c.285_295del XP_016866889.1:p.Arg96HisfsTer16
NM_003764.4:c.285_295del MANE Select NP_003755.2:p.Arg96HisfsTer16