Canonical Allele Identifier: CA129996171

Gene: G3BP1

Linked Data

• dbSNP Id: rs550099086
• gnomAD v3: 5-151805153-T-G
• gnomAD v4: 5-151805153-T-G
• MyVariant Identifiers: chr5:g.151184714T>G (hg19) ; chr5:g.151805153T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151805153T>G , CM000667.2:g.151805153T>G	GRCh38
NC_000005.9:g.151184714T>G , CM000667.1:g.151184714T>G	GRCh37
NC_000005.8:g.151164907T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356245.8:c.*1062T>G MANE Select	ENSP00000348578.3:n.*1062T>G
ENST00000520177.6:c.*1249T>G	ENSP00000427810.2:n.*1249T>G
ENST00000676634.1:n.834T>G
ENST00000676644.1:c.*2440T>G	ENSP00000504249.1:n.*2440T>G
ENST00000676715.1:c.970T>G
ENST00000676734.1:c.562+707T>G	ENSP00000504327.1:n.562+707T>G
ENST00000676878.1:c.562+707T>G	ENSP00000504118.1:n.562+707T>G
ENST00000676899.1:c.858T>G
ENST00000676911.1:n.832T>G
ENST00000676978.1:c.*819T>G	ENSP00000503939.1:n.*819T>G
ENST00000677323.1:c.*1062T>G	ENSP00000502880.1:n.*1062T>G
ENST00000677381.1:c.*2003T>G	ENSP00000504403.1:n.*2003T>G
ENST00000677493.1:c.*1538T>G	ENSP00000504786.1:n.*1538T>G
ENST00000677687.1:c.133-338T>G	ENSP00000504281.1:n.133-338T>G
ENST00000677757.1:n.4313T>G
ENST00000677923.1:c.*1501T>G	ENSP00000504573.1:n.*1501T>G
ENST00000678295.1:c.1067T>G	ENSP00000503775.1:n.1067T>G
ENST00000678646.1:c.*1062T>G	ENSP00000504525.1:n.*1062T>G
ENST00000678657.1:c.991T>G	ENSP00000504393.1:n.991T>G
ENST00000678854.1:c.*514T>G	ENSP00000503080.1:n.*514T>G
ENST00000678904.1:n.2842T>G
ENST00000678910.1:c.*798T>G	ENSP00000503654.1:n.*798T>G
ENST00000678925.1:c.*798T>G	ENSP00000503699.1:n.*798T>G
ENST00000678964.1:c.*1529T>G	ENSP00000503385.1:n.*1529T>G
ENST00000679289.1:c.*2067T>G	ENSP00000504039.1:n.*2067T>G
ENST00000356245.7:c.*1062T>G	ENSP00000348578.3:n.*1062T>G
ENST00000394123.7:c.*1062T>G	ENSP00000377681.3:n.*1062T>G
ENST00000520177.5:c.*2003T>G	ENSP00000427810.1:n.*2003T>G
NM_005754.2:c.*1062T>G	NP_005745.1:n.*1062T>G
NM_198395.1:c.*1062T>G	NP_938405.1:n.*1062T>G
XM_006714749.2:c.*1062T>G	XP_006714812.1:n.*1062T>G
XM_006714750.2:c.*1062T>G	XP_006714813.1:n.*1062T>G
NM_005754.3:c.*1062T>G MANE Select	NP_005745.1:n.*1062T>G
NM_198395.2:c.*1062T>G	NP_938405.1:n.*1062T>G