Canonical Allele Identifier: CA1591556985
Gene: G3BP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151805022A= , CM000667.2:g.151805022A= GRCh38
NC_000005.9:g.151184583A= , CM000667.1:g.151184583A= GRCh37
NC_000005.8:g.151164776A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356245.8:c.*931A= MANE Select ENSP00000348578.3:n.*931A=
ENST00000520177.6:c.*1118A= ENSP00000427810.2:n.*1118A=
ENST00000676634.1:n.703A=
ENST00000676644.1:c.*2309A= ENSP00000504249.1:n.*2309A=
ENST00000676715.1:c.839A=
ENST00000676734.1:c.562+576A= ENSP00000504327.1:n.562+576A=
ENST00000676878.1:c.562+576A= ENSP00000504118.1:n.562+576A=
ENST00000676899.1:c.727A=
ENST00000676911.1:n.701A=
ENST00000676978.1:c.*688A= ENSP00000503939.1:n.*688A=
ENST00000677323.1:c.*931A= ENSP00000502880.1:n.*931A=
ENST00000677381.1:c.*1872A= ENSP00000504403.1:n.*1872A=
ENST00000677493.1:c.*1407A= ENSP00000504786.1:n.*1407A=
ENST00000677687.1:c.133-469A= ENSP00000504281.1:n.133-469A=
ENST00000677757.1:n.4182A=
ENST00000677923.1:c.*1370A= ENSP00000504573.1:n.*1370A=
ENST00000678295.1:c.936A= ENSP00000503775.1:n.936A=
ENST00000678646.1:c.*931A= ENSP00000504525.1:n.*931A=
ENST00000678657.1:c.860A= ENSP00000504393.1:n.860A=
ENST00000678854.1:c.*383A= ENSP00000503080.1:n.*383A=
ENST00000678904.1:n.2711A=
ENST00000678910.1:c.*667A= ENSP00000503654.1:n.*667A=
ENST00000678925.1:c.*667A= ENSP00000503699.1:n.*667A=
ENST00000678964.1:c.*1398A= ENSP00000503385.1:n.*1398A=
ENST00000679289.1:c.*1936A= ENSP00000504039.1:n.*1936A=
ENST00000356245.7:c.*931A= ENSP00000348578.3:n.*931A=
ENST00000394123.7:c.*931A= ENSP00000377681.3:n.*931A=
ENST00000520177.5:c.*1872A= ENSP00000427810.1:n.*1872A=
NM_005754.2:c.*931A= NP_005745.1:n.*931A=
NM_198395.1:c.*931A= NP_938405.1:n.*931A=
XM_006714749.2:c.*931A= XP_006714812.1:n.*931A=
XM_006714750.2:c.*931A= XP_006714813.1:n.*931A=
NM_005754.3:c.*931A= MANE Select NP_005745.1:n.*931A=
NM_198395.2:c.*931A= NP_938405.1:n.*931A=