Canonical Allele Identifier: CA1591557030
Gene: G3BP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151805111G= , CM000667.2:g.151805111G= GRCh38
NC_000005.9:g.151184672G= , CM000667.1:g.151184672G= GRCh37
NC_000005.8:g.151164865G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356245.8:c.*1020G= MANE Select ENSP00000348578.3:n.*1020G=
ENST00000520177.6:c.*1207G= ENSP00000427810.2:n.*1207G=
ENST00000676634.1:n.792G=
ENST00000676644.1:c.*2398G= ENSP00000504249.1:n.*2398G=
ENST00000676715.1:c.928G=
ENST00000676734.1:c.562+665G= ENSP00000504327.1:n.562+665G=
ENST00000676878.1:c.562+665G= ENSP00000504118.1:n.562+665G=
ENST00000676899.1:c.816G=
ENST00000676911.1:n.790G=
ENST00000676978.1:c.*777G= ENSP00000503939.1:n.*777G=
ENST00000677323.1:c.*1020G= ENSP00000502880.1:n.*1020G=
ENST00000677381.1:c.*1961G= ENSP00000504403.1:n.*1961G=
ENST00000677493.1:c.*1496G= ENSP00000504786.1:n.*1496G=
ENST00000677687.1:c.133-380G= ENSP00000504281.1:n.133-380G=
ENST00000677757.1:n.4271G=
ENST00000677923.1:c.*1459G= ENSP00000504573.1:n.*1459G=
ENST00000678295.1:c.1025G= ENSP00000503775.1:n.1025G=
ENST00000678646.1:c.*1020G= ENSP00000504525.1:n.*1020G=
ENST00000678657.1:c.949G= ENSP00000504393.1:n.949G=
ENST00000678854.1:c.*472G= ENSP00000503080.1:n.*472G=
ENST00000678904.1:n.2800G=
ENST00000678910.1:c.*756G= ENSP00000503654.1:n.*756G=
ENST00000678925.1:c.*756G= ENSP00000503699.1:n.*756G=
ENST00000678964.1:c.*1487G= ENSP00000503385.1:n.*1487G=
ENST00000679289.1:c.*2025G= ENSP00000504039.1:n.*2025G=
ENST00000356245.7:c.*1020G= ENSP00000348578.3:n.*1020G=
ENST00000394123.7:c.*1020G= ENSP00000377681.3:n.*1020G=
ENST00000520177.5:c.*1961G= ENSP00000427810.1:n.*1961G=
NM_005754.2:c.*1020G= NP_005745.1:n.*1020G=
NM_198395.1:c.*1020G= NP_938405.1:n.*1020G=
XM_006714749.2:c.*1020G= XP_006714812.1:n.*1020G=
XM_006714750.2:c.*1020G= XP_006714813.1:n.*1020G=
NM_005754.3:c.*1020G= MANE Select NP_005745.1:n.*1020G=
NM_198395.2:c.*1020G= NP_938405.1:n.*1020G=