Canonical Allele Identifier: CA1591556976

Gene: G3BP1

Linked Data

• dbSNP Id: rs1309778187

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151805001_151805002del , CM000667.2:g.151805001_151805002del	GRCh38
NC_000005.9:g.151184562_151184563del , CM000667.1:g.151184562_151184563del	GRCh37
NC_000005.8:g.151164755_151164756del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356245.8:c.*910_*911del MANE Select	ENSP00000348578.3:n.*910_*911del
ENST00000520177.6:c.*1097_*1098del	ENSP00000427810.2:n.*1097_*1098del
ENST00000676634.1:n.682_683del
ENST00000676644.1:c.*2288_*2289del	ENSP00000504249.1:n.*2288_*2289del
ENST00000676715.1:c.818_819del
ENST00000676734.1:c.562+555_562+556del	ENSP00000504327.1:n.562+555_562+556del
ENST00000676878.1:c.562+555_562+556del	ENSP00000504118.1:n.562+555_562+556del
ENST00000676899.1:c.706_707del
ENST00000676911.1:n.680_681del
ENST00000676978.1:c.*667_*668del	ENSP00000503939.1:n.*667_*668del
ENST00000677323.1:c.*910_*911del	ENSP00000502880.1:n.*910_*911del
ENST00000677381.1:c.*1851_*1852del	ENSP00000504403.1:n.*1851_*1852del
ENST00000677493.1:c.*1386_*1387del	ENSP00000504786.1:n.*1386_*1387del
ENST00000677687.1:c.133-490_133-489del	ENSP00000504281.1:n.133-490_133-489del
ENST00000677757.1:n.4161_4162del
ENST00000677923.1:c.*1349_*1350del	ENSP00000504573.1:n.*1349_*1350del
ENST00000678295.1:c.915_916del	ENSP00000503775.1:n.915_916del
ENST00000678646.1:c.*910_*911del	ENSP00000504525.1:n.*910_*911del
ENST00000678657.1:c.839_840del	ENSP00000504393.1:n.839_840del
ENST00000678854.1:c.*362_*363del	ENSP00000503080.1:n.*362_*363del
ENST00000678904.1:n.2690_2691del
ENST00000678910.1:c.*646_*647del	ENSP00000503654.1:n.*646_*647del
ENST00000678925.1:c.*646_*647del	ENSP00000503699.1:n.*646_*647del
ENST00000678964.1:c.*1377_*1378del	ENSP00000503385.1:n.*1377_*1378del
ENST00000679289.1:c.*1915_*1916del	ENSP00000504039.1:n.*1915_*1916del
ENST00000356245.7:c.*910_*911del	ENSP00000348578.3:n.*910_*911del
ENST00000394123.7:c.*910_*911del	ENSP00000377681.3:n.*910_*911del
ENST00000520177.5:c.*1851_*1852del	ENSP00000427810.1:n.*1851_*1852del
NM_005754.2:c.*910_*911del	NP_005745.1:n.*910_*911del
NM_198395.1:c.*910_*911del	NP_938405.1:n.*910_*911del
XM_006714749.2:c.*910_*911del	XP_006714812.1:n.*910_*911del
XM_006714750.2:c.*910_*911del	XP_006714813.1:n.*910_*911del
NM_005754.3:c.*910_*911del MANE Select	NP_005745.1:n.*910_*911del
NM_198395.2:c.*910_*911del	NP_938405.1:n.*910_*911del