Canonical Allele Identifier: CA365948719
Gene: STX11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2056496
ClinVar RCV Id: RCV002947513
dbSNP Id: rs1204079066

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.144186818G>A , CM000668.2:g.144186818G>A GRCh38
NC_000006.11:g.144507955G>A , CM000668.1:g.144507955G>A GRCh37
NC_000006.10:g.144549648G>A NCBI36
NG_007613.1:g.41302G>A , LRG_113:g.41302G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698355.1:c.191G>A ENSP00000513678.1:p.Arg64Gln
ENST00000698356.1:c.191G>A ENSP00000513679.1:p.Arg64Gln
ENST00000698357.1:c.191G>A ENSP00000513680.1:p.Arg64Gln
ENST00000367568.5:c.191G>A MANE Select ENSP00000356540.4:p.Arg64Gln
ENST00000367568.4:c.191G>A ENSP00000356540.4:p.Arg64Gln
NM_003764.3:c.191G>A , LRG_113t1:c.191G>A NP_003755.2:p.Arg64Gln
XM_011536213.1:c.269G>A XP_011534515.1:p.Arg90Gln
XM_011536214.1:c.191G>A XP_011534516.1:p.Arg64Gln
XM_011536215.1:c.191G>A XP_011534517.1:p.Arg64Gln
XM_011536216.1:c.191G>A XP_011534518.1:p.Arg64Gln
XM_011536217.1:c.191G>A XP_011534519.1:p.Arg64Gln
XM_011536218.1:c.191G>A XP_011534520.1:p.Arg64Gln
XM_011536213.2:c.269G>A XP_011534515.1:p.Arg90Gln
XM_011536214.2:c.191G>A XP_011534516.1:p.Arg64Gln
XM_011536217.2:c.191G>A XP_011534519.1:p.Arg64Gln
XM_011536218.2:c.191G>A XP_011534520.1:p.Arg64Gln
XM_017011400.1:c.191G>A XP_016866889.1:p.Arg64Gln
NM_003764.4:c.191G>A MANE Select NP_003755.2:p.Arg64Gln