Canonical Allele Identifier: CA805712391

Gene: G3BP1

Linked Data

• dbSNP Id: rs1481914287
• gnomAD v3: 5-151805104-C-CTTT
• gnomAD v4: 5-151805104-C-CTTT
• MyVariant Identifiers: chr5:g.151184665_151184666insTTT (hg19) ; chr5:g.151805104_151805105insTTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151805105_151805106insTTT , CM000667.2:g.151805105_151805106insTTT	GRCh38
NC_000005.9:g.151184666_151184667insTTT , CM000667.1:g.151184666_151184667insTTT	GRCh37
NC_000005.8:g.151164859_151164860insTTT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356245.8:c.*1014_*1015insTTT MANE Select	ENSP00000348578.3:n.*1014_*1015insTTT
ENST00000520177.6:c.*1201_*1202insTTT	ENSP00000427810.2:n.*1201_*1202insTTT
ENST00000676634.1:n.786_787insTTT
ENST00000676644.1:c.*2392_*2393insTTT	ENSP00000504249.1:n.*2392_*2393insTTT
ENST00000676715.1:c.922_923insTTT
ENST00000676734.1:c.562+659_562+660insTTT	ENSP00000504327.1:n.562+659_562+660insTTT
ENST00000676878.1:c.562+659_562+660insTTT	ENSP00000504118.1:n.562+659_562+660insTTT
ENST00000676899.1:c.810_811insTTT
ENST00000676911.1:n.784_785insTTT
ENST00000676978.1:c.*771_*772insTTT	ENSP00000503939.1:n.*771_*772insTTT
ENST00000677323.1:c.*1014_*1015insTTT	ENSP00000502880.1:n.*1014_*1015insTTT
ENST00000677381.1:c.*1955_*1956insTTT	ENSP00000504403.1:n.*1955_*1956insTTT
ENST00000677493.1:c.*1490_*1491insTTT	ENSP00000504786.1:n.*1490_*1491insTTT
ENST00000677687.1:c.133-386_133-385insTTT	ENSP00000504281.1:n.133-386_133-385insTTT
ENST00000677757.1:n.4265_4266insTTT
ENST00000677923.1:c.*1453_*1454insTTT	ENSP00000504573.1:n.*1453_*1454insTTT
ENST00000678295.1:c.1019_1020insTTT	ENSP00000503775.1:n.1019_1020insTTT
ENST00000678646.1:c.*1014_*1015insTTT	ENSP00000504525.1:n.*1014_*1015insTTT
ENST00000678657.1:c.943_944insTTT	ENSP00000504393.1:n.943_944insTTT
ENST00000678854.1:c.*466_*467insTTT	ENSP00000503080.1:n.*466_*467insTTT
ENST00000678904.1:n.2794_2795insTTT
ENST00000678910.1:c.*750_*751insTTT	ENSP00000503654.1:n.*750_*751insTTT
ENST00000678925.1:c.*750_*751insTTT	ENSP00000503699.1:n.*750_*751insTTT
ENST00000678964.1:c.*1481_*1482insTTT	ENSP00000503385.1:n.*1481_*1482insTTT
ENST00000679289.1:c.*2019_*2020insTTT	ENSP00000504039.1:n.*2019_*2020insTTT
ENST00000356245.7:c.*1014_*1015insTTT	ENSP00000348578.3:n.*1014_*1015insTTT
ENST00000394123.7:c.*1014_*1015insTTT	ENSP00000377681.3:n.*1014_*1015insTTT
ENST00000520177.5:c.*1955_*1956insTTT	ENSP00000427810.1:n.*1955_*1956insTTT
NM_005754.2:c.*1014_*1015insTTT	NP_005745.1:n.*1014_*1015insTTT
NM_198395.1:c.*1014_*1015insTTT	NP_938405.1:n.*1014_*1015insTTT
XM_006714749.2:c.*1014_*1015insTTT	XP_006714812.1:n.*1014_*1015insTTT
XM_006714750.2:c.*1014_*1015insTTT	XP_006714813.1:n.*1014_*1015insTTT
NM_005754.3:c.*1014_*1015insTTT MANE Select	NP_005745.1:n.*1014_*1015insTTT
NM_198395.2:c.*1014_*1015insTTT	NP_938405.1:n.*1014_*1015insTTT