Canonical Allele Identifier: CA1082962807

Gene: G3BP1

Linked Data

• dbSNP Id: rs1762920223
• gnomAD v3: 5-151805088-A-G
• gnomAD v4: 5-151805088-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151805088A>G , CM000667.2:g.151805088A>G	GRCh38
NC_000005.9:g.151184649A>G , CM000667.1:g.151184649A>G	GRCh37
NC_000005.8:g.151164842A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356245.8:c.*997A>G MANE Select	ENSP00000348578.3:n.*997A>G
ENST00000520177.6:c.*1184A>G	ENSP00000427810.2:n.*1184A>G
ENST00000676634.1:n.769A>G
ENST00000676644.1:c.*2375A>G	ENSP00000504249.1:n.*2375A>G
ENST00000676715.1:c.905A>G
ENST00000676734.1:c.562+642A>G	ENSP00000504327.1:n.562+642A>G
ENST00000676878.1:c.562+642A>G	ENSP00000504118.1:n.562+642A>G
ENST00000676899.1:c.793A>G
ENST00000676911.1:n.767A>G
ENST00000676978.1:c.*754A>G	ENSP00000503939.1:n.*754A>G
ENST00000677323.1:c.*997A>G	ENSP00000502880.1:n.*997A>G
ENST00000677381.1:c.*1938A>G	ENSP00000504403.1:n.*1938A>G
ENST00000677493.1:c.*1473A>G	ENSP00000504786.1:n.*1473A>G
ENST00000677687.1:c.133-403A>G	ENSP00000504281.1:n.133-403A>G
ENST00000677757.1:n.4248A>G
ENST00000677923.1:c.*1436A>G	ENSP00000504573.1:n.*1436A>G
ENST00000678295.1:c.1002A>G	ENSP00000503775.1:n.1002A>G
ENST00000678646.1:c.*997A>G	ENSP00000504525.1:n.*997A>G
ENST00000678657.1:c.926A>G	ENSP00000504393.1:n.926A>G
ENST00000678854.1:c.*449A>G	ENSP00000503080.1:n.*449A>G
ENST00000678904.1:n.2777A>G
ENST00000678910.1:c.*733A>G	ENSP00000503654.1:n.*733A>G
ENST00000678925.1:c.*733A>G	ENSP00000503699.1:n.*733A>G
ENST00000678964.1:c.*1464A>G	ENSP00000503385.1:n.*1464A>G
ENST00000679289.1:c.*2002A>G	ENSP00000504039.1:n.*2002A>G
ENST00000356245.7:c.*997A>G	ENSP00000348578.3:n.*997A>G
ENST00000394123.7:c.*997A>G	ENSP00000377681.3:n.*997A>G
ENST00000520177.5:c.*1938A>G	ENSP00000427810.1:n.*1938A>G
NM_005754.2:c.*997A>G	NP_005745.1:n.*997A>G
NM_198395.1:c.*997A>G	NP_938405.1:n.*997A>G
XM_006714749.2:c.*997A>G	XP_006714812.1:n.*997A>G
XM_006714750.2:c.*997A>G	XP_006714813.1:n.*997A>G
NM_005754.3:c.*997A>G MANE Select	NP_005745.1:n.*997A>G
NM_198395.2:c.*997A>G	NP_938405.1:n.*997A>G