Canonical Allele Identifier: CA650907176

Gene: G3BP1

Linked Data

• COSMIC: COSN20091288

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151805164_151805165insT , CM000667.2:g.151805164_151805165insT	GRCh38
NC_000005.9:g.151184725_151184726insT , CM000667.1:g.151184725_151184726insT	GRCh37
NC_000005.8:g.151164918_151164919insT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356245.8:c.*1073_*1074insT MANE Select	ENSP00000348578.3:n.*1073_*1074insT
ENST00000520177.6:c.*1260_*1261insT	ENSP00000427810.2:n.*1260_*1261insT
ENST00000676634.1:n.845_846insT
ENST00000676644.1:c.*2451_*2452insT	ENSP00000504249.1:n.*2451_*2452insT
ENST00000676715.1:c.981_982insT
ENST00000676734.1:c.562+718_562+719insT	ENSP00000504327.1:n.562+718_562+719insT
ENST00000676878.1:c.562+718_562+719insT	ENSP00000504118.1:n.562+718_562+719insT
ENST00000676899.1:c.869_870insT
ENST00000676911.1:n.843_844insT
ENST00000676978.1:c.*830_*831insT	ENSP00000503939.1:n.*830_*831insT
ENST00000677323.1:c.*1073_*1074insT	ENSP00000502880.1:n.*1073_*1074insT
ENST00000677381.1:c.*2014_*2015insT	ENSP00000504403.1:n.*2014_*2015insT
ENST00000677493.1:c.*1549_*1550insT	ENSP00000504786.1:n.*1549_*1550insT
ENST00000677687.1:c.133-327_133-326insT	ENSP00000504281.1:n.133-327_133-326insT
ENST00000677757.1:n.4324_4325insT
ENST00000677923.1:c.*1512_*1513insT	ENSP00000504573.1:n.*1512_*1513insT
ENST00000678295.1:c.1078_1079insT	ENSP00000503775.1:n.1078_1079insT
ENST00000678646.1:c.*1073_*1074insT	ENSP00000504525.1:n.*1073_*1074insT
ENST00000678657.1:c.1002_1003insT	ENSP00000504393.1:n.1002_1003insT
ENST00000678854.1:c.*525_*526insT	ENSP00000503080.1:n.*525_*526insT
ENST00000678904.1:n.2853_2854insT
ENST00000678910.1:c.*809_*810insT	ENSP00000503654.1:n.*809_*810insT
ENST00000678925.1:c.*809_*810insT	ENSP00000503699.1:n.*809_*810insT
ENST00000678964.1:c.*1540_*1541insT	ENSP00000503385.1:n.*1540_*1541insT
ENST00000679289.1:c.*2078_*2079insT	ENSP00000504039.1:n.*2078_*2079insT
ENST00000356245.7:c.*1073_*1074insT	ENSP00000348578.3:n.*1073_*1074insT
ENST00000394123.7:c.*1073_*1074insT	ENSP00000377681.3:n.*1073_*1074insT
ENST00000520177.5:c.*2014_*2015insT	ENSP00000427810.1:n.*2014_*2015insT
NM_005754.2:c.*1073_*1074insT	NP_005745.1:n.*1073_*1074insT
NM_198395.1:c.*1073_*1074insT	NP_938405.1:n.*1073_*1074insT
XM_006714749.2:c.*1073_*1074insT	XP_006714812.1:n.*1073_*1074insT
XM_006714750.2:c.*1073_*1074insT	XP_006714813.1:n.*1073_*1074insT
NM_005754.3:c.*1073_*1074insT MANE Select	NP_005745.1:n.*1073_*1074insT
NM_198395.2:c.*1073_*1074insT	NP_938405.1:n.*1073_*1074insT