Canonical Allele Identifier: CA2539121742

Gene: STING1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139480761_139480766del , CM000667.2:g.139480761_139480766del	GRCh38
NC_000005.9:g.138860346_138860351del , CM000667.1:g.138860346_138860351del	GRCh37
NC_000005.8:g.138840530_138840535del	NCBI36
NG_034249.1:g.7025_7030del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330794.9:c.520+24_520+29del MANE Select	ENSP00000331288.4:n.520+24_520+29del
ENST00000502362.2:n.1295+24_1295+29del
ENST00000510817.2:c.520+24_520+29del	ENSP00000427455.2:n.520+24_520+29del
ENST00000511886.6:n.1462+24_1462+29del
ENST00000512606.6:n.756+24_756+29del
ENST00000514119.6:n.739+24_739+29del
ENST00000650883.1:c.163+24_163+29del	ENSP00000499142.1:n.163+24_163+29del
ENST00000651565.1:c.163+24_163+29del	ENSP00000498768.1:n.163+24_163+29del
ENST00000651699.1:c.520+24_520+29del	ENSP00000499166.1:n.520+24_520+29del
ENST00000652110.1:c.520+24_520+29del	ENSP00000498513.1:n.520+24_520+29del
ENST00000652271.1:c.520+24_520+29del	ENSP00000498596.1:n.520+24_520+29del
ENST00000652543.1:c.163+24_163+29del	ENSP00000498683.1:n.163+24_163+29del
ENST00000330794.8:c.520+24_520+29del	ENSP00000331288.4:n.520+24_520+29del
ENST00000502825.1:n.298+24_298+29del
ENST00000503287.5:n.412+24_412+29del
ENST00000503838.1:n.560+24_560+29del
ENST00000507297.5:n.1157+24_1157+29del
ENST00000509573.5:n.319+24_319+29del
ENST00000510817.1:c.520+24_520+29del	ENSP00000427455.1:n.520+24_520+29del
ENST00000511850.1:n.742+24_742+29del
ENST00000511886.5:n.526+24_526+29del
ENST00000512606.5:n.445+24_445+29del
ENST00000514119.5:n.957+24_957+29del
ENST00000515507.5:n.566+24_566+29del
NM_001301738.1:c.520+24_520+29del	NP_001288667.1:n.520+24_520+29del
NM_198282.3:c.520+24_520+29del	NP_938023.1:n.520+24_520+29del
XM_005268445.2:c.520+24_520+29del	XP_005268502.1:n.520+24_520+29del
XM_011537639.1:c.520+24_520+29del	XP_011535941.1:n.520+24_520+29del
XM_011537640.1:c.163+24_163+29del	XP_011535942.1:n.163+24_163+29del
XM_005268445.4:c.520+24_520+29del	XP_005268502.1:n.520+24_520+29del
XM_011537639.3:c.520+24_520+29del	XP_011535941.1:n.520+24_520+29del
XM_011537640.2:c.163+24_163+29del	XP_011535942.1:n.163+24_163+29del
NM_001301738.2:c.520+24_520+29del	NP_001288667.1:n.520+24_520+29del
NM_001367258.1:c.163+24_163+29del	NP_001354187.1:n.163+24_163+29del
NM_198282.4:c.520+24_520+29del MANE Select	NP_938023.1:n.520+24_520+29del