Canonical Allele Identifier: CA1591557065

Gene: G3BP1

Linked Data

• dbSNP Id: rs1762922756

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151805204G>A , CM000667.2:g.151805204G>A	GRCh38
NC_000005.9:g.151184765G>A , CM000667.1:g.151184765G>A	GRCh37
NC_000005.8:g.151164958G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356245.8:c.*1113G>A MANE Select	ENSP00000348578.3:n.*1113G>A
ENST00000520177.6:c.*1300G>A	ENSP00000427810.2:n.*1300G>A
ENST00000676634.1:n.885G>A
ENST00000676644.1:c.*2491G>A	ENSP00000504249.1:n.*2491G>A
ENST00000676715.1:c.1021G>A
ENST00000676734.1:c.562+758G>A	ENSP00000504327.1:n.562+758G>A
ENST00000676878.1:c.562+758G>A	ENSP00000504118.1:n.562+758G>A
ENST00000676899.1:c.909G>A
ENST00000676911.1:n.883G>A
ENST00000676978.1:c.*870G>A	ENSP00000503939.1:n.*870G>A
ENST00000677323.1:c.*1113G>A	ENSP00000502880.1:n.*1113G>A
ENST00000677381.1:c.*2054G>A	ENSP00000504403.1:n.*2054G>A
ENST00000677493.1:c.*1589G>A	ENSP00000504786.1:n.*1589G>A
ENST00000677687.1:c.133-287G>A	ENSP00000504281.1:n.133-287G>A
ENST00000677757.1:n.4364G>A
ENST00000677923.1:c.*1552G>A	ENSP00000504573.1:n.*1552G>A
ENST00000678295.1:c.1118G>A	ENSP00000503775.1:n.1118G>A
ENST00000678646.1:c.*1113G>A	ENSP00000504525.1:n.*1113G>A
ENST00000678657.1:c.1042G>A	ENSP00000504393.1:n.1042G>A
ENST00000678854.1:c.*565G>A	ENSP00000503080.1:n.*565G>A
ENST00000678904.1:n.2893G>A
ENST00000678910.1:c.*849G>A	ENSP00000503654.1:n.*849G>A
ENST00000678925.1:c.*849G>A	ENSP00000503699.1:n.*849G>A
ENST00000678964.1:c.*1580G>A	ENSP00000503385.1:n.*1580G>A
ENST00000679289.1:c.*2118G>A	ENSP00000504039.1:n.*2118G>A
ENST00000356245.7:c.*1113G>A	ENSP00000348578.3:n.*1113G>A
ENST00000394123.7:c.*1113G>A	ENSP00000377681.3:n.*1113G>A
ENST00000520177.5:c.*2054G>A	ENSP00000427810.1:n.*2054G>A
NM_005754.2:c.*1113G>A	NP_005745.1:n.*1113G>A
NM_198395.1:c.*1113G>A	NP_938405.1:n.*1113G>A
XM_006714749.2:c.*1113G>A	XP_006714812.1:n.*1113G>A
XM_006714750.2:c.*1113G>A	XP_006714813.1:n.*1113G>A
NM_005754.3:c.*1113G>A MANE Select	NP_005745.1:n.*1113G>A
NM_198395.2:c.*1113G>A	NP_938405.1:n.*1113G>A