Canonical Allele Identifier: CA1591557028
Gene: G3BP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151805109T= , CM000667.2:g.151805109T= GRCh38
NC_000005.9:g.151184670T= , CM000667.1:g.151184670T= GRCh37
NC_000005.8:g.151164863T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356245.8:c.*1018T= MANE Select ENSP00000348578.3:n.*1018T=
ENST00000520177.6:c.*1205T= ENSP00000427810.2:n.*1205T=
ENST00000676634.1:n.790T=
ENST00000676644.1:c.*2396T= ENSP00000504249.1:n.*2396T=
ENST00000676715.1:c.926T=
ENST00000676734.1:c.562+663T= ENSP00000504327.1:n.562+663T=
ENST00000676878.1:c.562+663T= ENSP00000504118.1:n.562+663T=
ENST00000676899.1:c.814T=
ENST00000676911.1:n.788T=
ENST00000676978.1:c.*775T= ENSP00000503939.1:n.*775T=
ENST00000677323.1:c.*1018T= ENSP00000502880.1:n.*1018T=
ENST00000677381.1:c.*1959T= ENSP00000504403.1:n.*1959T=
ENST00000677493.1:c.*1494T= ENSP00000504786.1:n.*1494T=
ENST00000677687.1:c.133-382T= ENSP00000504281.1:n.133-382T=
ENST00000677757.1:n.4269T=
ENST00000677923.1:c.*1457T= ENSP00000504573.1:n.*1457T=
ENST00000678295.1:c.1023T= ENSP00000503775.1:n.1023T=
ENST00000678646.1:c.*1018T= ENSP00000504525.1:n.*1018T=
ENST00000678657.1:c.947T= ENSP00000504393.1:n.947T=
ENST00000678854.1:c.*470T= ENSP00000503080.1:n.*470T=
ENST00000678904.1:n.2798T=
ENST00000678910.1:c.*754T= ENSP00000503654.1:n.*754T=
ENST00000678925.1:c.*754T= ENSP00000503699.1:n.*754T=
ENST00000678964.1:c.*1485T= ENSP00000503385.1:n.*1485T=
ENST00000679289.1:c.*2023T= ENSP00000504039.1:n.*2023T=
ENST00000356245.7:c.*1018T= ENSP00000348578.3:n.*1018T=
ENST00000394123.7:c.*1018T= ENSP00000377681.3:n.*1018T=
ENST00000520177.5:c.*1959T= ENSP00000427810.1:n.*1959T=
NM_005754.2:c.*1018T= NP_005745.1:n.*1018T=
NM_198395.1:c.*1018T= NP_938405.1:n.*1018T=
XM_006714749.2:c.*1018T= XP_006714812.1:n.*1018T=
XM_006714750.2:c.*1018T= XP_006714813.1:n.*1018T=
NM_005754.3:c.*1018T= MANE Select NP_005745.1:n.*1018T=
NM_198395.2:c.*1018T= NP_938405.1:n.*1018T=