Canonical Allele Identifier: CA129996155

Gene: G3BP1

Linked Data

• dbSNP Id: rs760997900
• MyVariant Identifiers: chr5:g.151184697_151184698insTATC (hg19) ; chr5:g.151805136_151805137insTATC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151805139_151805142dup , CM000667.2:g.151805139_151805142dup	GRCh38
NC_000005.9:g.151184700_151184703dup , CM000667.1:g.151184700_151184703dup	GRCh37
NC_000005.8:g.151164893_151164896dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356245.8:c.*1048_*1051dup MANE Select	ENSP00000348578.3:n.*1048_*1051dup
ENST00000520177.6:c.*1235_*1238dup	ENSP00000427810.2:n.*1235_*1238dup
ENST00000676634.1:n.820_823dup
ENST00000676644.1:c.*2426_*2429dup	ENSP00000504249.1:n.*2426_*2429dup
ENST00000676715.1:c.956_959dup
ENST00000676734.1:c.562+693_562+696dup	ENSP00000504327.1:n.562+693_562+696dup
ENST00000676878.1:c.562+693_562+696dup	ENSP00000504118.1:n.562+693_562+696dup
ENST00000676899.1:c.844_847dup
ENST00000676911.1:n.818_821dup
ENST00000676978.1:c.*805_*808dup	ENSP00000503939.1:n.*805_*808dup
ENST00000677323.1:c.*1048_*1051dup	ENSP00000502880.1:n.*1048_*1051dup
ENST00000677381.1:c.*1989_*1992dup	ENSP00000504403.1:n.*1989_*1992dup
ENST00000677493.1:c.*1524_*1527dup	ENSP00000504786.1:n.*1524_*1527dup
ENST00000677687.1:c.133-352_133-349dup	ENSP00000504281.1:n.133-352_133-349dup
ENST00000677757.1:n.4299_4302dup
ENST00000677923.1:c.*1487_*1490dup	ENSP00000504573.1:n.*1487_*1490dup
ENST00000678295.1:c.1053_1056dup	ENSP00000503775.1:n.1053_1056dup
ENST00000678646.1:c.*1048_*1051dup	ENSP00000504525.1:n.*1048_*1051dup
ENST00000678657.1:c.977_980dup	ENSP00000504393.1:n.977_980dup
ENST00000678854.1:c.*500_*503dup	ENSP00000503080.1:n.*500_*503dup
ENST00000678904.1:n.2828_2831dup
ENST00000678910.1:c.*784_*787dup	ENSP00000503654.1:n.*784_*787dup
ENST00000678925.1:c.*784_*787dup	ENSP00000503699.1:n.*784_*787dup
ENST00000678964.1:c.*1515_*1518dup	ENSP00000503385.1:n.*1515_*1518dup
ENST00000679289.1:c.*2053_*2056dup	ENSP00000504039.1:n.*2053_*2056dup
ENST00000356245.7:c.*1048_*1051dup	ENSP00000348578.3:n.*1048_*1051dup
ENST00000394123.7:c.*1048_*1051dup	ENSP00000377681.3:n.*1048_*1051dup
ENST00000520177.5:c.*1989_*1992dup	ENSP00000427810.1:n.*1989_*1992dup
NM_005754.2:c.*1048_*1051dup	NP_005745.1:n.*1048_*1051dup
NM_198395.1:c.*1048_*1051dup	NP_938405.1:n.*1048_*1051dup
XM_006714749.2:c.*1048_*1051dup	XP_006714812.1:n.*1048_*1051dup
XM_006714750.2:c.*1048_*1051dup	XP_006714813.1:n.*1048_*1051dup
NM_005754.3:c.*1048_*1051dup MANE Select	NP_005745.1:n.*1048_*1051dup
NM_198395.2:c.*1048_*1051dup	NP_938405.1:n.*1048_*1051dup