Canonical Allele Identifier: CA563631023

Gene: G3BP1

Linked Data

• dbSNP Id: rs1171318043
• gnomAD v2: 5-151184610-G-T
• gnomAD v3: 5-151805049-G-T
• gnomAD v4: 5-151805049-G-T
• MyVariant Identifiers: chr5:g.151184610G>T (hg19) ; chr5:g.151805049G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151805049G>T , CM000667.2:g.151805049G>T	GRCh38
NC_000005.9:g.151184610G>T , CM000667.1:g.151184610G>T	GRCh37
NC_000005.8:g.151164803G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356245.8:c.*958G>T MANE Select	ENSP00000348578.3:n.*958G>T
ENST00000520177.6:c.*1145G>T	ENSP00000427810.2:n.*1145G>T
ENST00000676634.1:n.730G>T
ENST00000676644.1:c.*2336G>T	ENSP00000504249.1:n.*2336G>T
ENST00000676715.1:c.866G>T
ENST00000676734.1:c.562+603G>T	ENSP00000504327.1:n.562+603G>T
ENST00000676878.1:c.562+603G>T	ENSP00000504118.1:n.562+603G>T
ENST00000676899.1:c.754G>T
ENST00000676911.1:n.728G>T
ENST00000676978.1:c.*715G>T	ENSP00000503939.1:n.*715G>T
ENST00000677323.1:c.*958G>T	ENSP00000502880.1:n.*958G>T
ENST00000677381.1:c.*1899G>T	ENSP00000504403.1:n.*1899G>T
ENST00000677493.1:c.*1434G>T	ENSP00000504786.1:n.*1434G>T
ENST00000677687.1:c.133-442G>T	ENSP00000504281.1:n.133-442G>T
ENST00000677757.1:n.4209G>T
ENST00000677923.1:c.*1397G>T	ENSP00000504573.1:n.*1397G>T
ENST00000678295.1:c.963G>T	ENSP00000503775.1:n.963G>T
ENST00000678646.1:c.*958G>T	ENSP00000504525.1:n.*958G>T
ENST00000678657.1:c.887G>T	ENSP00000504393.1:n.887G>T
ENST00000678854.1:c.*410G>T	ENSP00000503080.1:n.*410G>T
ENST00000678904.1:n.2738G>T
ENST00000678910.1:c.*694G>T	ENSP00000503654.1:n.*694G>T
ENST00000678925.1:c.*694G>T	ENSP00000503699.1:n.*694G>T
ENST00000678964.1:c.*1425G>T	ENSP00000503385.1:n.*1425G>T
ENST00000679289.1:c.*1963G>T	ENSP00000504039.1:n.*1963G>T
ENST00000356245.7:c.*958G>T	ENSP00000348578.3:n.*958G>T
ENST00000394123.7:c.*958G>T	ENSP00000377681.3:n.*958G>T
ENST00000520177.5:c.*1899G>T	ENSP00000427810.1:n.*1899G>T
NM_005754.2:c.*958G>T	NP_005745.1:n.*958G>T
NM_198395.1:c.*958G>T	NP_938405.1:n.*958G>T
XM_006714749.2:c.*958G>T	XP_006714812.1:n.*958G>T
XM_006714750.2:c.*958G>T	XP_006714813.1:n.*958G>T
NM_005754.3:c.*958G>T MANE Select	NP_005745.1:n.*958G>T
NM_198395.2:c.*958G>T	NP_938405.1:n.*958G>T