Canonical Allele Identifier: CA1591557027
Gene: G3BP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151805108A= , CM000667.2:g.151805108A= GRCh38
NC_000005.9:g.151184669A= , CM000667.1:g.151184669A= GRCh37
NC_000005.8:g.151164862A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356245.8:c.*1017A= MANE Select ENSP00000348578.3:n.*1017A=
ENST00000520177.6:c.*1204A= ENSP00000427810.2:n.*1204A=
ENST00000676634.1:n.789A=
ENST00000676644.1:c.*2395A= ENSP00000504249.1:n.*2395A=
ENST00000676715.1:c.925A=
ENST00000676734.1:c.562+662A= ENSP00000504327.1:n.562+662A=
ENST00000676878.1:c.562+662A= ENSP00000504118.1:n.562+662A=
ENST00000676899.1:c.813A=
ENST00000676911.1:n.787A=
ENST00000676978.1:c.*774A= ENSP00000503939.1:n.*774A=
ENST00000677323.1:c.*1017A= ENSP00000502880.1:n.*1017A=
ENST00000677381.1:c.*1958A= ENSP00000504403.1:n.*1958A=
ENST00000677493.1:c.*1493A= ENSP00000504786.1:n.*1493A=
ENST00000677687.1:c.133-383A= ENSP00000504281.1:n.133-383A=
ENST00000677757.1:n.4268A=
ENST00000677923.1:c.*1456A= ENSP00000504573.1:n.*1456A=
ENST00000678295.1:c.1022A= ENSP00000503775.1:n.1022A=
ENST00000678646.1:c.*1017A= ENSP00000504525.1:n.*1017A=
ENST00000678657.1:c.946A= ENSP00000504393.1:n.946A=
ENST00000678854.1:c.*469A= ENSP00000503080.1:n.*469A=
ENST00000678904.1:n.2797A=
ENST00000678910.1:c.*753A= ENSP00000503654.1:n.*753A=
ENST00000678925.1:c.*753A= ENSP00000503699.1:n.*753A=
ENST00000678964.1:c.*1484A= ENSP00000503385.1:n.*1484A=
ENST00000679289.1:c.*2022A= ENSP00000504039.1:n.*2022A=
ENST00000356245.7:c.*1017A= ENSP00000348578.3:n.*1017A=
ENST00000394123.7:c.*1017A= ENSP00000377681.3:n.*1017A=
ENST00000520177.5:c.*1958A= ENSP00000427810.1:n.*1958A=
NM_005754.2:c.*1017A= NP_005745.1:n.*1017A=
NM_198395.1:c.*1017A= NP_938405.1:n.*1017A=
XM_006714749.2:c.*1017A= XP_006714812.1:n.*1017A=
XM_006714750.2:c.*1017A= XP_006714813.1:n.*1017A=
NM_005754.3:c.*1017A= MANE Select NP_005745.1:n.*1017A=
NM_198395.2:c.*1017A= NP_938405.1:n.*1017A=