Canonical Allele Identifier: CA1591557031
Gene: G3BP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151805114C= , CM000667.2:g.151805114C= GRCh38
NC_000005.9:g.151184675C= , CM000667.1:g.151184675C= GRCh37
NC_000005.8:g.151164868C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356245.8:c.*1023C= MANE Select ENSP00000348578.3:n.*1023C=
ENST00000520177.6:c.*1210C= ENSP00000427810.2:n.*1210C=
ENST00000676634.1:n.795C=
ENST00000676644.1:c.*2401C= ENSP00000504249.1:n.*2401C=
ENST00000676715.1:c.931C=
ENST00000676734.1:c.562+668C= ENSP00000504327.1:n.562+668C=
ENST00000676878.1:c.562+668C= ENSP00000504118.1:n.562+668C=
ENST00000676899.1:c.819C=
ENST00000676911.1:n.793C=
ENST00000676978.1:c.*780C= ENSP00000503939.1:n.*780C=
ENST00000677323.1:c.*1023C= ENSP00000502880.1:n.*1023C=
ENST00000677381.1:c.*1964C= ENSP00000504403.1:n.*1964C=
ENST00000677493.1:c.*1499C= ENSP00000504786.1:n.*1499C=
ENST00000677687.1:c.133-377C= ENSP00000504281.1:n.133-377C=
ENST00000677757.1:n.4274C=
ENST00000677923.1:c.*1462C= ENSP00000504573.1:n.*1462C=
ENST00000678295.1:c.1028C= ENSP00000503775.1:n.1028C=
ENST00000678646.1:c.*1023C= ENSP00000504525.1:n.*1023C=
ENST00000678657.1:c.952C= ENSP00000504393.1:n.952C=
ENST00000678854.1:c.*475C= ENSP00000503080.1:n.*475C=
ENST00000678904.1:n.2803C=
ENST00000678910.1:c.*759C= ENSP00000503654.1:n.*759C=
ENST00000678925.1:c.*759C= ENSP00000503699.1:n.*759C=
ENST00000678964.1:c.*1490C= ENSP00000503385.1:n.*1490C=
ENST00000679289.1:c.*2028C= ENSP00000504039.1:n.*2028C=
ENST00000356245.7:c.*1023C= ENSP00000348578.3:n.*1023C=
ENST00000394123.7:c.*1023C= ENSP00000377681.3:n.*1023C=
ENST00000520177.5:c.*1964C= ENSP00000427810.1:n.*1964C=
NM_005754.2:c.*1023C= NP_005745.1:n.*1023C=
NM_198395.1:c.*1023C= NP_938405.1:n.*1023C=
XM_006714749.2:c.*1023C= XP_006714812.1:n.*1023C=
XM_006714750.2:c.*1023C= XP_006714813.1:n.*1023C=
NM_005754.3:c.*1023C= MANE Select NP_005745.1:n.*1023C=
NM_198395.2:c.*1023C= NP_938405.1:n.*1023C=