Canonical Allele Identifier: CA2675539870
Gene: STING1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.139480761_139480764dup , CM000667.2:g.139480761_139480764dup GRCh38
NC_000005.9:g.138860346_138860349dup , CM000667.1:g.138860346_138860349dup GRCh37
NC_000005.8:g.138840530_138840533dup NCBI36
NG_034249.1:g.7027_7030dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000330794.9:c.520+26_520+29dup MANE Select ENSP00000331288.4:n.520+26_520+29dup
ENST00000502362.2:n.1295+26_1295+29dup
ENST00000510817.2:c.520+26_520+29dup ENSP00000427455.2:n.520+26_520+29dup
ENST00000511886.6:n.1462+26_1462+29dup
ENST00000512606.6:n.756+26_756+29dup
ENST00000514119.6:n.739+26_739+29dup
ENST00000650883.1:c.163+26_163+29dup ENSP00000499142.1:n.163+26_163+29dup
ENST00000651565.1:c.163+26_163+29dup ENSP00000498768.1:n.163+26_163+29dup
ENST00000651699.1:c.520+26_520+29dup ENSP00000499166.1:n.520+26_520+29dup
ENST00000652110.1:c.520+26_520+29dup ENSP00000498513.1:n.520+26_520+29dup
ENST00000652271.1:c.520+26_520+29dup ENSP00000498596.1:n.520+26_520+29dup
ENST00000652543.1:c.163+26_163+29dup ENSP00000498683.1:n.163+26_163+29dup
ENST00000330794.8:c.520+26_520+29dup ENSP00000331288.4:n.520+26_520+29dup
ENST00000502825.1:n.298+26_298+29dup
ENST00000503287.5:n.412+26_412+29dup
ENST00000503838.1:n.560+26_560+29dup
ENST00000507297.5:n.1157+26_1157+29dup
ENST00000509573.5:n.319+26_319+29dup
ENST00000510817.1:c.520+26_520+29dup ENSP00000427455.1:n.520+26_520+29dup
ENST00000511850.1:n.742+26_742+29dup
ENST00000511886.5:n.526+26_526+29dup
ENST00000512606.5:n.445+26_445+29dup
ENST00000514119.5:n.957+26_957+29dup
ENST00000515507.5:n.566+26_566+29dup
NM_001301738.1:c.520+26_520+29dup NP_001288667.1:n.520+26_520+29dup
NM_198282.3:c.520+26_520+29dup NP_938023.1:n.520+26_520+29dup
XM_005268445.2:c.520+26_520+29dup XP_005268502.1:n.520+26_520+29dup
XM_011537639.1:c.520+26_520+29dup XP_011535941.1:n.520+26_520+29dup
XM_011537640.1:c.163+26_163+29dup XP_011535942.1:n.163+26_163+29dup
XM_005268445.4:c.520+26_520+29dup XP_005268502.1:n.520+26_520+29dup
XM_011537639.3:c.520+26_520+29dup XP_011535941.1:n.520+26_520+29dup
XM_011537640.2:c.163+26_163+29dup XP_011535942.1:n.163+26_163+29dup
NM_001301738.2:c.520+26_520+29dup NP_001288667.1:n.520+26_520+29dup
NM_001367258.1:c.163+26_163+29dup NP_001354187.1:n.163+26_163+29dup
NM_198282.4:c.520+26_520+29dup MANE Select NP_938023.1:n.520+26_520+29dup