Canonical Allele Identifier: CA1591556970
Gene: G3BP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151804986C= , CM000667.2:g.151804986C= GRCh38
NC_000005.9:g.151184547C= , CM000667.1:g.151184547C= GRCh37
NC_000005.8:g.151164740C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356245.8:c.*895C= MANE Select ENSP00000348578.3:n.*895C=
ENST00000520177.6:c.*1082C= ENSP00000427810.2:n.*1082C=
ENST00000676634.1:n.667C=
ENST00000676644.1:c.*2273C= ENSP00000504249.1:n.*2273C=
ENST00000676715.1:c.803C=
ENST00000676734.1:c.562+540C= ENSP00000504327.1:n.562+540C=
ENST00000676878.1:c.562+540C= ENSP00000504118.1:n.562+540C=
ENST00000676899.1:c.691C=
ENST00000676911.1:n.665C=
ENST00000676978.1:c.*652C= ENSP00000503939.1:n.*652C=
ENST00000677323.1:c.*895C= ENSP00000502880.1:n.*895C=
ENST00000677381.1:c.*1836C= ENSP00000504403.1:n.*1836C=
ENST00000677493.1:c.*1371C= ENSP00000504786.1:n.*1371C=
ENST00000677687.1:c.133-505C= ENSP00000504281.1:n.133-505C=
ENST00000677757.1:n.4146C=
ENST00000677923.1:c.*1334C= ENSP00000504573.1:n.*1334C=
ENST00000678295.1:c.900C= ENSP00000503775.1:n.900C=
ENST00000678646.1:c.*895C= ENSP00000504525.1:n.*895C=
ENST00000678657.1:c.824C= ENSP00000504393.1:n.824C=
ENST00000678854.1:c.*347C= ENSP00000503080.1:n.*347C=
ENST00000678904.1:n.2675C=
ENST00000678910.1:c.*631C= ENSP00000503654.1:n.*631C=
ENST00000678925.1:c.*631C= ENSP00000503699.1:n.*631C=
ENST00000678964.1:c.*1362C= ENSP00000503385.1:n.*1362C=
ENST00000679289.1:c.*1900C= ENSP00000504039.1:n.*1900C=
ENST00000356245.7:c.*895C= ENSP00000348578.3:n.*895C=
ENST00000394123.7:c.*895C= ENSP00000377681.3:n.*895C=
ENST00000520177.5:c.*1836C= ENSP00000427810.1:n.*1836C=
NM_005754.2:c.*895C= NP_005745.1:n.*895C=
NM_198395.1:c.*895C= NP_938405.1:n.*895C=
XM_006714749.2:c.*895C= XP_006714812.1:n.*895C=
XM_006714750.2:c.*895C= XP_006714813.1:n.*895C=
NM_005754.3:c.*895C= MANE Select NP_005745.1:n.*895C=
NM_198395.2:c.*895C= NP_938405.1:n.*895C=