Canonical Allele Identifier: CA1591556975

Gene: G3BP1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151804999_151805001delinsCTT , CM000667.2:g.151804999_151805001delinsCTT	GRCh38
NC_000005.9:g.151184560_151184562delinsCTT , CM000667.1:g.151184560_151184562delinsCTT	GRCh37
NC_000005.8:g.151164753_151164755delinsCTT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356245.8:c.*908_*910delinsCTT MANE Select	ENSP00000348578.3:n.*908_*910delinsCTT
ENST00000520177.6:c.*1095_*1097delinsCTT	ENSP00000427810.2:n.*1095_*1097delinsCTT
ENST00000676634.1:n.680_682delinsCTT
ENST00000676644.1:c.*2286_*2288delinsCTT	ENSP00000504249.1:n.*2286_*2288delinsCTT
ENST00000676715.1:c.816_818delinsCTT
ENST00000676734.1:c.562+553_562+555delinsCTT	ENSP00000504327.1:n.562+553_562+555delinsCTT
ENST00000676878.1:c.562+553_562+555delinsCTT	ENSP00000504118.1:n.562+553_562+555delinsCTT
ENST00000676899.1:c.704_706delinsCTT
ENST00000676911.1:n.678_680delinsCTT
ENST00000676978.1:c.*665_*667delinsCTT	ENSP00000503939.1:n.*665_*667delinsCTT
ENST00000677323.1:c.*908_*910delinsCTT	ENSP00000502880.1:n.*908_*910delinsCTT
ENST00000677381.1:c.*1849_*1851delinsCTT	ENSP00000504403.1:n.*1849_*1851delinsCTT
ENST00000677493.1:c.*1384_*1386delinsCTT	ENSP00000504786.1:n.*1384_*1386delinsCTT
ENST00000677687.1:c.133-492_133-490delinsCTT	ENSP00000504281.1:n.133-492_133-490delinsCTT
ENST00000677757.1:n.4159_4161delinsCTT
ENST00000677923.1:c.*1347_*1349delinsCTT	ENSP00000504573.1:n.*1347_*1349delinsCTT
ENST00000678295.1:c.913_915delinsCTT	ENSP00000503775.1:n.913_915delinsCTT
ENST00000678646.1:c.*908_*910delinsCTT	ENSP00000504525.1:n.*908_*910delinsCTT
ENST00000678657.1:c.837_839delinsCTT	ENSP00000504393.1:n.837_839delinsCTT
ENST00000678854.1:c.*360_*362delinsCTT	ENSP00000503080.1:n.*360_*362delinsCTT
ENST00000678904.1:n.2688_2690delinsCTT
ENST00000678910.1:c.*644_*646delinsCTT	ENSP00000503654.1:n.*644_*646delinsCTT
ENST00000678925.1:c.*644_*646delinsCTT	ENSP00000503699.1:n.*644_*646delinsCTT
ENST00000678964.1:c.*1375_*1377delinsCTT	ENSP00000503385.1:n.*1375_*1377delinsCTT
ENST00000679289.1:c.*1913_*1915delinsCTT	ENSP00000504039.1:n.*1913_*1915delinsCTT
ENST00000356245.7:c.*908_*910delinsCTT	ENSP00000348578.3:n.*908_*910delinsCTT
ENST00000394123.7:c.*908_*910delinsCTT	ENSP00000377681.3:n.*908_*910delinsCTT
ENST00000520177.5:c.*1849_*1851delinsCTT	ENSP00000427810.1:n.*1849_*1851delinsCTT
NM_005754.2:c.*908_*910delinsCTT	NP_005745.1:n.*908_*910delinsCTT
NM_198395.1:c.*908_*910delinsCTT	NP_938405.1:n.*908_*910delinsCTT
XM_006714749.2:c.*908_*910delinsCTT	XP_006714812.1:n.*908_*910delinsCTT
XM_006714750.2:c.*908_*910delinsCTT	XP_006714813.1:n.*908_*910delinsCTT
NM_005754.3:c.*908_*910delinsCTT MANE Select	NP_005745.1:n.*908_*910delinsCTT
NM_198395.2:c.*908_*910delinsCTT	NP_938405.1:n.*908_*910delinsCTT