Canonical Allele Identifier: CA1591557010

Gene: G3BP1

Linked Data

• dbSNP Id: rs1762919199

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151805061G>T , CM000667.2:g.151805061G>T	GRCh38
NC_000005.9:g.151184622G>T , CM000667.1:g.151184622G>T	GRCh37
NC_000005.8:g.151164815G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356245.8:c.*970G>T MANE Select	ENSP00000348578.3:n.*970G>T
ENST00000520177.6:c.*1157G>T	ENSP00000427810.2:n.*1157G>T
ENST00000676634.1:n.742G>T
ENST00000676644.1:c.*2348G>T	ENSP00000504249.1:n.*2348G>T
ENST00000676715.1:c.878G>T
ENST00000676734.1:c.562+615G>T	ENSP00000504327.1:n.562+615G>T
ENST00000676878.1:c.562+615G>T	ENSP00000504118.1:n.562+615G>T
ENST00000676899.1:c.766G>T
ENST00000676911.1:n.740G>T
ENST00000676978.1:c.*727G>T	ENSP00000503939.1:n.*727G>T
ENST00000677323.1:c.*970G>T	ENSP00000502880.1:n.*970G>T
ENST00000677381.1:c.*1911G>T	ENSP00000504403.1:n.*1911G>T
ENST00000677493.1:c.*1446G>T	ENSP00000504786.1:n.*1446G>T
ENST00000677687.1:c.133-430G>T	ENSP00000504281.1:n.133-430G>T
ENST00000677757.1:n.4221G>T
ENST00000677923.1:c.*1409G>T	ENSP00000504573.1:n.*1409G>T
ENST00000678295.1:c.975G>T	ENSP00000503775.1:n.975G>T
ENST00000678646.1:c.*970G>T	ENSP00000504525.1:n.*970G>T
ENST00000678657.1:c.899G>T	ENSP00000504393.1:n.899G>T
ENST00000678854.1:c.*422G>T	ENSP00000503080.1:n.*422G>T
ENST00000678904.1:n.2750G>T
ENST00000678910.1:c.*706G>T	ENSP00000503654.1:n.*706G>T
ENST00000678925.1:c.*706G>T	ENSP00000503699.1:n.*706G>T
ENST00000678964.1:c.*1437G>T	ENSP00000503385.1:n.*1437G>T
ENST00000679289.1:c.*1975G>T	ENSP00000504039.1:n.*1975G>T
ENST00000356245.7:c.*970G>T	ENSP00000348578.3:n.*970G>T
ENST00000394123.7:c.*970G>T	ENSP00000377681.3:n.*970G>T
ENST00000520177.5:c.*1911G>T	ENSP00000427810.1:n.*1911G>T
NM_005754.2:c.*970G>T	NP_005745.1:n.*970G>T
NM_198395.1:c.*970G>T	NP_938405.1:n.*970G>T
XM_006714749.2:c.*970G>T	XP_006714812.1:n.*970G>T
XM_006714750.2:c.*970G>T	XP_006714813.1:n.*970G>T
NM_005754.3:c.*970G>T MANE Select	NP_005745.1:n.*970G>T
NM_198395.2:c.*970G>T	NP_938405.1:n.*970G>T