Canonical Allele Identifier: CA2676107727

Gene: G3BP1

Linked Data

• gnomAD v4: 5-151805120-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151805120T>A , CM000667.2:g.151805120T>A	GRCh38
NC_000005.9:g.151184681T>A , CM000667.1:g.151184681T>A	GRCh37
NC_000005.8:g.151164874T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356245.8:c.*1029T>A MANE Select	ENSP00000348578.3:n.*1029T>A
ENST00000520177.6:c.*1216T>A	ENSP00000427810.2:n.*1216T>A
ENST00000676634.1:n.801T>A
ENST00000676644.1:c.*2407T>A	ENSP00000504249.1:n.*2407T>A
ENST00000676715.1:c.937T>A
ENST00000676734.1:c.562+674T>A	ENSP00000504327.1:n.562+674T>A
ENST00000676878.1:c.562+674T>A	ENSP00000504118.1:n.562+674T>A
ENST00000676899.1:c.825T>A
ENST00000676911.1:n.799T>A
ENST00000676978.1:c.*786T>A	ENSP00000503939.1:n.*786T>A
ENST00000677323.1:c.*1029T>A	ENSP00000502880.1:n.*1029T>A
ENST00000677381.1:c.*1970T>A	ENSP00000504403.1:n.*1970T>A
ENST00000677493.1:c.*1505T>A	ENSP00000504786.1:n.*1505T>A
ENST00000677687.1:c.133-371T>A	ENSP00000504281.1:n.133-371T>A
ENST00000677757.1:n.4280T>A
ENST00000677923.1:c.*1468T>A	ENSP00000504573.1:n.*1468T>A
ENST00000678295.1:c.1034T>A	ENSP00000503775.1:n.1034T>A
ENST00000678646.1:c.*1029T>A	ENSP00000504525.1:n.*1029T>A
ENST00000678657.1:c.958T>A	ENSP00000504393.1:n.958T>A
ENST00000678854.1:c.*481T>A	ENSP00000503080.1:n.*481T>A
ENST00000678904.1:n.2809T>A
ENST00000678910.1:c.*765T>A	ENSP00000503654.1:n.*765T>A
ENST00000678925.1:c.*765T>A	ENSP00000503699.1:n.*765T>A
ENST00000678964.1:c.*1496T>A	ENSP00000503385.1:n.*1496T>A
ENST00000679289.1:c.*2034T>A	ENSP00000504039.1:n.*2034T>A
ENST00000356245.7:c.*1029T>A	ENSP00000348578.3:n.*1029T>A
ENST00000394123.7:c.*1029T>A	ENSP00000377681.3:n.*1029T>A
ENST00000520177.5:c.*1970T>A	ENSP00000427810.1:n.*1970T>A
NM_005754.2:c.*1029T>A	NP_005745.1:n.*1029T>A
NM_198395.1:c.*1029T>A	NP_938405.1:n.*1029T>A
XM_006714749.2:c.*1029T>A	XP_006714812.1:n.*1029T>A
XM_006714750.2:c.*1029T>A	XP_006714813.1:n.*1029T>A
NM_005754.3:c.*1029T>A MANE Select	NP_005745.1:n.*1029T>A
NM_198395.2:c.*1029T>A	NP_938405.1:n.*1029T>A