Canonical Allele Identifier: CA2710197790

Gene: G3BP1

Linked Data

• dbSNP Id: rs2113256715

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151805152del , CM000667.2:g.151805152del	GRCh38
NC_000005.9:g.151184713del , CM000667.1:g.151184713del	GRCh37
NC_000005.8:g.151164906del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356245.8:c.*1061del MANE Select	ENSP00000348578.3:n.*1061del
ENST00000520177.6:c.*1248del	ENSP00000427810.2:n.*1248del
ENST00000676634.1:n.833del
ENST00000676644.1:c.*2439del	ENSP00000504249.1:n.*2439del
ENST00000676715.1:c.969del
ENST00000676734.1:c.562+706del	ENSP00000504327.1:n.562+706del
ENST00000676878.1:c.562+706del	ENSP00000504118.1:n.562+706del
ENST00000676899.1:c.857del
ENST00000676911.1:n.831del
ENST00000676978.1:c.*818del	ENSP00000503939.1:n.*818del
ENST00000677323.1:c.*1061del	ENSP00000502880.1:n.*1061del
ENST00000677381.1:c.*2002del	ENSP00000504403.1:n.*2002del
ENST00000677493.1:c.*1537del	ENSP00000504786.1:n.*1537del
ENST00000677687.1:c.133-339del	ENSP00000504281.1:n.133-339del
ENST00000677757.1:n.4312del
ENST00000677923.1:c.*1500del	ENSP00000504573.1:n.*1500del
ENST00000678295.1:c.1066del	ENSP00000503775.1:n.1066del
ENST00000678646.1:c.*1061del	ENSP00000504525.1:n.*1061del
ENST00000678657.1:c.990del	ENSP00000504393.1:n.990del
ENST00000678854.1:c.*513del	ENSP00000503080.1:n.*513del
ENST00000678904.1:n.2841del
ENST00000678910.1:c.*797del	ENSP00000503654.1:n.*797del
ENST00000678925.1:c.*797del	ENSP00000503699.1:n.*797del
ENST00000678964.1:c.*1528del	ENSP00000503385.1:n.*1528del
ENST00000679289.1:c.*2066del	ENSP00000504039.1:n.*2066del
ENST00000356245.7:c.*1061del	ENSP00000348578.3:n.*1061del
ENST00000394123.7:c.*1061del	ENSP00000377681.3:n.*1061del
ENST00000520177.5:c.*2002del	ENSP00000427810.1:n.*2002del
NM_005754.2:c.*1061del	NP_005745.1:n.*1061del
NM_198395.1:c.*1061del	NP_938405.1:n.*1061del
XM_006714749.2:c.*1061del	XP_006714812.1:n.*1061del
XM_006714750.2:c.*1061del	XP_006714813.1:n.*1061del
NM_005754.3:c.*1061del MANE Select	NP_005745.1:n.*1061del
NM_198395.2:c.*1061del	NP_938405.1:n.*1061del