Canonical Allele Identifier: CA365948814
Gene: STX11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.144186866G>C , CM000668.2:g.144186866G>C GRCh38
NC_000006.11:g.144508003G>C , CM000668.1:g.144508003G>C GRCh37
NC_000006.10:g.144549696G>C NCBI36
NG_007613.1:g.41350G>C , LRG_113:g.41350G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698355.1:c.239G>C ENSP00000513678.1:p.Ser80Thr
ENST00000698356.1:c.239G>C ENSP00000513679.1:p.Ser80Thr
ENST00000698357.1:c.239G>C ENSP00000513680.1:p.Ser80Thr
ENST00000367568.5:c.239G>C MANE Select ENSP00000356540.4:p.Ser80Thr
ENST00000367568.4:c.239G>C ENSP00000356540.4:p.Ser80Thr
NM_003764.3:c.239G>C , LRG_113t1:c.239G>C NP_003755.2:p.Ser80Thr
XM_011536213.1:c.317G>C XP_011534515.1:p.Ser106Thr
XM_011536214.1:c.239G>C XP_011534516.1:p.Ser80Thr
XM_011536215.1:c.239G>C XP_011534517.1:p.Ser80Thr
XM_011536216.1:c.239G>C XP_011534518.1:p.Ser80Thr
XM_011536217.1:c.239G>C XP_011534519.1:p.Ser80Thr
XM_011536218.1:c.239G>C XP_011534520.1:p.Ser80Thr
XM_011536213.2:c.317G>C XP_011534515.1:p.Ser106Thr
XM_011536214.2:c.239G>C XP_011534516.1:p.Ser80Thr
XM_011536217.2:c.239G>C XP_011534519.1:p.Ser80Thr
XM_011536218.2:c.239G>C XP_011534520.1:p.Ser80Thr
XM_017011400.1:c.239G>C XP_016866889.1:p.Ser80Thr
NM_003764.4:c.239G>C MANE Select NP_003755.2:p.Ser80Thr