Canonical Allele Identifier: CA1669582448
Gene: STX11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.144186690C= , CM000668.2:g.144186690C= GRCh38
NC_000006.11:g.144507827C= , CM000668.1:g.144507827C= GRCh37
NC_000006.10:g.144549520C= NCBI36
NG_007613.1:g.41174C= , LRG_113:g.41174C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698355.1:c.63C= ENSP00000513678.1:p.Asp21=
ENST00000698356.1:c.63C= ENSP00000513679.1:p.Asp21=
ENST00000698357.1:c.63C= ENSP00000513680.1:p.Asp21=
ENST00000367568.5:c.63C= MANE Select ENSP00000356540.4:p.Asp21=
ENST00000367568.4:c.63C= ENSP00000356540.4:p.Asp21=
NM_003764.3:c.63C= , LRG_113t1:c.63C= NP_003755.2:p.Asp21=
XM_011536213.1:c.141C= XP_011534515.1:p.Asp47=
XM_011536214.1:c.63C= XP_011534516.1:p.Asp21=
XM_011536215.1:c.63C= XP_011534517.1:p.Asp21=
XM_011536216.1:c.63C= XP_011534518.1:p.Asp21=
XM_011536217.1:c.63C= XP_011534519.1:p.Asp21=
XM_011536218.1:c.63C= XP_011534520.1:p.Asp21=
XM_011536213.2:c.141C= XP_011534515.1:p.Asp47=
XM_011536214.2:c.63C= XP_011534516.1:p.Asp21=
XM_011536217.2:c.63C= XP_011534519.1:p.Asp21=
XM_011536218.2:c.63C= XP_011534520.1:p.Asp21=
XM_017011400.1:c.63C= XP_016866889.1:p.Asp21=
NM_003764.4:c.63C= MANE Select NP_003755.2:p.Asp21=