Canonical Allele Identifier: CA1082962785

Gene: G3BP1

Linked Data

• dbSNP Id: rs1762917698
• gnomAD v3: 5-151804999-C-G
• gnomAD v4: 5-151804999-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151804999C>G , CM000667.2:g.151804999C>G	GRCh38
NC_000005.9:g.151184560C>G , CM000667.1:g.151184560C>G	GRCh37
NC_000005.8:g.151164753C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356245.8:c.*908C>G MANE Select	ENSP00000348578.3:n.*908C>G
ENST00000520177.6:c.*1095C>G	ENSP00000427810.2:n.*1095C>G
ENST00000676634.1:n.680C>G
ENST00000676644.1:c.*2286C>G	ENSP00000504249.1:n.*2286C>G
ENST00000676715.1:c.816C>G
ENST00000676734.1:c.562+553C>G	ENSP00000504327.1:n.562+553C>G
ENST00000676878.1:c.562+553C>G	ENSP00000504118.1:n.562+553C>G
ENST00000676899.1:c.704C>G
ENST00000676911.1:n.678C>G
ENST00000676978.1:c.*665C>G	ENSP00000503939.1:n.*665C>G
ENST00000677323.1:c.*908C>G	ENSP00000502880.1:n.*908C>G
ENST00000677381.1:c.*1849C>G	ENSP00000504403.1:n.*1849C>G
ENST00000677493.1:c.*1384C>G	ENSP00000504786.1:n.*1384C>G
ENST00000677687.1:c.133-492C>G	ENSP00000504281.1:n.133-492C>G
ENST00000677757.1:n.4159C>G
ENST00000677923.1:c.*1347C>G	ENSP00000504573.1:n.*1347C>G
ENST00000678295.1:c.913C>G	ENSP00000503775.1:n.913C>G
ENST00000678646.1:c.*908C>G	ENSP00000504525.1:n.*908C>G
ENST00000678657.1:c.837C>G	ENSP00000504393.1:n.837C>G
ENST00000678854.1:c.*360C>G	ENSP00000503080.1:n.*360C>G
ENST00000678904.1:n.2688C>G
ENST00000678910.1:c.*644C>G	ENSP00000503654.1:n.*644C>G
ENST00000678925.1:c.*644C>G	ENSP00000503699.1:n.*644C>G
ENST00000678964.1:c.*1375C>G	ENSP00000503385.1:n.*1375C>G
ENST00000679289.1:c.*1913C>G	ENSP00000504039.1:n.*1913C>G
ENST00000356245.7:c.*908C>G	ENSP00000348578.3:n.*908C>G
ENST00000394123.7:c.*908C>G	ENSP00000377681.3:n.*908C>G
ENST00000520177.5:c.*1849C>G	ENSP00000427810.1:n.*1849C>G
NM_005754.2:c.*908C>G	NP_005745.1:n.*908C>G
NM_198395.1:c.*908C>G	NP_938405.1:n.*908C>G
XM_006714749.2:c.*908C>G	XP_006714812.1:n.*908C>G
XM_006714750.2:c.*908C>G	XP_006714813.1:n.*908C>G
NM_005754.3:c.*908C>G MANE Select	NP_005745.1:n.*908C>G
NM_198395.2:c.*908C>G	NP_938405.1:n.*908C>G