Canonical Allele Identifier: CA1591557032

Gene: G3BP1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151805124_151805125delinsAT , CM000667.2:g.151805124_151805125delinsAT	GRCh38
NC_000005.9:g.151184685_151184686delinsAT , CM000667.1:g.151184685_151184686delinsAT	GRCh37
NC_000005.8:g.151164878_151164879delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356245.8:c.*1033_*1034delinsAT MANE Select	ENSP00000348578.3:n.*1033_*1034delinsAT
ENST00000520177.6:c.*1220_*1221delinsAT	ENSP00000427810.2:n.*1220_*1221delinsAT
ENST00000676634.1:n.805_806delinsAT
ENST00000676644.1:c.*2411_*2412delinsAT	ENSP00000504249.1:n.*2411_*2412delinsAT
ENST00000676715.1:c.941_942delinsAT
ENST00000676734.1:c.562+678_562+679delinsAT	ENSP00000504327.1:n.562+678_562+679delinsAT
ENST00000676878.1:c.562+678_562+679delinsAT	ENSP00000504118.1:n.562+678_562+679delinsAT
ENST00000676899.1:c.829_830delinsAT
ENST00000676911.1:n.803_804delinsAT
ENST00000676978.1:c.*790_*791delinsAT	ENSP00000503939.1:n.*790_*791delinsAT
ENST00000677323.1:c.*1033_*1034delinsAT	ENSP00000502880.1:n.*1033_*1034delinsAT
ENST00000677381.1:c.*1974_*1975delinsAT	ENSP00000504403.1:n.*1974_*1975delinsAT
ENST00000677493.1:c.*1509_*1510delinsAT	ENSP00000504786.1:n.*1509_*1510delinsAT
ENST00000677687.1:c.133-367_133-366delinsAT	ENSP00000504281.1:n.133-367_133-366delinsAT
ENST00000677757.1:n.4284_4285delinsAT
ENST00000677923.1:c.*1472_*1473delinsAT	ENSP00000504573.1:n.*1472_*1473delinsAT
ENST00000678295.1:c.1038_1039delinsAT	ENSP00000503775.1:n.1038_1039delinsAT
ENST00000678646.1:c.*1033_*1034delinsAT	ENSP00000504525.1:n.*1033_*1034delinsAT
ENST00000678657.1:c.962_963delinsAT	ENSP00000504393.1:n.962_963delinsAT
ENST00000678854.1:c.*485_*486delinsAT	ENSP00000503080.1:n.*485_*486delinsAT
ENST00000678904.1:n.2813_2814delinsAT
ENST00000678910.1:c.*769_*770delinsAT	ENSP00000503654.1:n.*769_*770delinsAT
ENST00000678925.1:c.*769_*770delinsAT	ENSP00000503699.1:n.*769_*770delinsAT
ENST00000678964.1:c.*1500_*1501delinsAT	ENSP00000503385.1:n.*1500_*1501delinsAT
ENST00000679289.1:c.*2038_*2039delinsAT	ENSP00000504039.1:n.*2038_*2039delinsAT
ENST00000356245.7:c.*1033_*1034delinsAT	ENSP00000348578.3:n.*1033_*1034delinsAT
ENST00000394123.7:c.*1033_*1034delinsAT	ENSP00000377681.3:n.*1033_*1034delinsAT
ENST00000520177.5:c.*1974_*1975delinsAT	ENSP00000427810.1:n.*1974_*1975delinsAT
NM_005754.2:c.*1033_*1034delinsAT	NP_005745.1:n.*1033_*1034delinsAT
NM_198395.1:c.*1033_*1034delinsAT	NP_938405.1:n.*1033_*1034delinsAT
XM_006714749.2:c.*1033_*1034delinsAT	XP_006714812.1:n.*1033_*1034delinsAT
XM_006714750.2:c.*1033_*1034delinsAT	XP_006714813.1:n.*1033_*1034delinsAT
NM_005754.3:c.*1033_*1034delinsAT MANE Select	NP_005745.1:n.*1033_*1034delinsAT
NM_198395.2:c.*1033_*1034delinsAT	NP_938405.1:n.*1033_*1034delinsAT