Canonical Allele Identifier: CA1591556967
Gene: G3BP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151804981A= , CM000667.2:g.151804981A= GRCh38
NC_000005.9:g.151184542A= , CM000667.1:g.151184542A= GRCh37
NC_000005.8:g.151164735A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356245.8:c.*890A= MANE Select ENSP00000348578.3:n.*890A=
ENST00000520177.6:c.*1077A= ENSP00000427810.2:n.*1077A=
ENST00000676634.1:n.662A=
ENST00000676644.1:c.*2268A= ENSP00000504249.1:n.*2268A=
ENST00000676715.1:c.798A=
ENST00000676734.1:c.562+535A= ENSP00000504327.1:n.562+535A=
ENST00000676878.1:c.562+535A= ENSP00000504118.1:n.562+535A=
ENST00000676899.1:c.686A=
ENST00000676911.1:n.660A=
ENST00000676978.1:c.*647A= ENSP00000503939.1:n.*647A=
ENST00000677323.1:c.*890A= ENSP00000502880.1:n.*890A=
ENST00000677381.1:c.*1831A= ENSP00000504403.1:n.*1831A=
ENST00000677493.1:c.*1366A= ENSP00000504786.1:n.*1366A=
ENST00000677687.1:c.133-510A= ENSP00000504281.1:n.133-510A=
ENST00000677757.1:n.4141A=
ENST00000677923.1:c.*1329A= ENSP00000504573.1:n.*1329A=
ENST00000678295.1:c.895A= ENSP00000503775.1:n.895A=
ENST00000678646.1:c.*890A= ENSP00000504525.1:n.*890A=
ENST00000678657.1:c.819A= ENSP00000504393.1:n.819A=
ENST00000678854.1:c.*342A= ENSP00000503080.1:n.*342A=
ENST00000678904.1:n.2670A=
ENST00000678910.1:c.*626A= ENSP00000503654.1:n.*626A=
ENST00000678925.1:c.*626A= ENSP00000503699.1:n.*626A=
ENST00000678964.1:c.*1357A= ENSP00000503385.1:n.*1357A=
ENST00000679289.1:c.*1895A= ENSP00000504039.1:n.*1895A=
ENST00000356245.7:c.*890A= ENSP00000348578.3:n.*890A=
ENST00000394123.7:c.*890A= ENSP00000377681.3:n.*890A=
ENST00000520177.5:c.*1831A= ENSP00000427810.1:n.*1831A=
NM_005754.2:c.*890A= NP_005745.1:n.*890A=
NM_198395.1:c.*890A= NP_938405.1:n.*890A=
XM_006714749.2:c.*890A= XP_006714812.1:n.*890A=
XM_006714750.2:c.*890A= XP_006714813.1:n.*890A=
NM_005754.3:c.*890A= MANE Select NP_005745.1:n.*890A=
NM_198395.2:c.*890A= NP_938405.1:n.*890A=