Canonical Allele Identifier: CA1591557036
Gene: G3BP1 HGNC NCBI

Linked Data

dbSNP Id: rs1762920783

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151805130A>G , CM000667.2:g.151805130A>G GRCh38
NC_000005.9:g.151184691A>G , CM000667.1:g.151184691A>G GRCh37
NC_000005.8:g.151164884A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356245.8:c.*1039A>G MANE Select ENSP00000348578.3:n.*1039A>G
ENST00000520177.6:c.*1226A>G ENSP00000427810.2:n.*1226A>G
ENST00000676634.1:n.811A>G
ENST00000676644.1:c.*2417A>G ENSP00000504249.1:n.*2417A>G
ENST00000676715.1:c.947A>G
ENST00000676734.1:c.562+684A>G ENSP00000504327.1:n.562+684A>G
ENST00000676878.1:c.562+684A>G ENSP00000504118.1:n.562+684A>G
ENST00000676899.1:c.835A>G
ENST00000676911.1:n.809A>G
ENST00000676978.1:c.*796A>G ENSP00000503939.1:n.*796A>G
ENST00000677323.1:c.*1039A>G ENSP00000502880.1:n.*1039A>G
ENST00000677381.1:c.*1980A>G ENSP00000504403.1:n.*1980A>G
ENST00000677493.1:c.*1515A>G ENSP00000504786.1:n.*1515A>G
ENST00000677687.1:c.133-361A>G ENSP00000504281.1:n.133-361A>G
ENST00000677757.1:n.4290A>G
ENST00000677923.1:c.*1478A>G ENSP00000504573.1:n.*1478A>G
ENST00000678295.1:c.1044A>G ENSP00000503775.1:n.1044A>G
ENST00000678646.1:c.*1039A>G ENSP00000504525.1:n.*1039A>G
ENST00000678657.1:c.968A>G ENSP00000504393.1:n.968A>G
ENST00000678854.1:c.*491A>G ENSP00000503080.1:n.*491A>G
ENST00000678904.1:n.2819A>G
ENST00000678910.1:c.*775A>G ENSP00000503654.1:n.*775A>G
ENST00000678925.1:c.*775A>G ENSP00000503699.1:n.*775A>G
ENST00000678964.1:c.*1506A>G ENSP00000503385.1:n.*1506A>G
ENST00000679289.1:c.*2044A>G ENSP00000504039.1:n.*2044A>G
ENST00000356245.7:c.*1039A>G ENSP00000348578.3:n.*1039A>G
ENST00000394123.7:c.*1039A>G ENSP00000377681.3:n.*1039A>G
ENST00000520177.5:c.*1980A>G ENSP00000427810.1:n.*1980A>G
NM_005754.2:c.*1039A>G NP_005745.1:n.*1039A>G
NM_198395.1:c.*1039A>G NP_938405.1:n.*1039A>G
XM_006714749.2:c.*1039A>G XP_006714812.1:n.*1039A>G
XM_006714750.2:c.*1039A>G XP_006714813.1:n.*1039A>G
NM_005754.3:c.*1039A>G MANE Select NP_005745.1:n.*1039A>G
NM_198395.2:c.*1039A>G NP_938405.1:n.*1039A>G