Canonical Allele Identifier: CA1591557044
Gene: G3BP1 HGNC NCBI

Linked Data

dbSNP Id: rs1762921312

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151805146A>C , CM000667.2:g.151805146A>C GRCh38
NC_000005.9:g.151184707A>C , CM000667.1:g.151184707A>C GRCh37
NC_000005.8:g.151164900A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356245.8:c.*1055A>C MANE Select ENSP00000348578.3:n.*1055A>C
ENST00000520177.6:c.*1242A>C ENSP00000427810.2:n.*1242A>C
ENST00000676634.1:n.827A>C
ENST00000676644.1:c.*2433A>C ENSP00000504249.1:n.*2433A>C
ENST00000676715.1:c.963A>C
ENST00000676734.1:c.562+700A>C ENSP00000504327.1:n.562+700A>C
ENST00000676878.1:c.562+700A>C ENSP00000504118.1:n.562+700A>C
ENST00000676899.1:c.851A>C
ENST00000676911.1:n.825A>C
ENST00000676978.1:c.*812A>C ENSP00000503939.1:n.*812A>C
ENST00000677323.1:c.*1055A>C ENSP00000502880.1:n.*1055A>C
ENST00000677381.1:c.*1996A>C ENSP00000504403.1:n.*1996A>C
ENST00000677493.1:c.*1531A>C ENSP00000504786.1:n.*1531A>C
ENST00000677687.1:c.133-345A>C ENSP00000504281.1:n.133-345A>C
ENST00000677757.1:n.4306A>C
ENST00000677923.1:c.*1494A>C ENSP00000504573.1:n.*1494A>C
ENST00000678295.1:c.1060A>C ENSP00000503775.1:n.1060A>C
ENST00000678646.1:c.*1055A>C ENSP00000504525.1:n.*1055A>C
ENST00000678657.1:c.984A>C ENSP00000504393.1:n.984A>C
ENST00000678854.1:c.*507A>C ENSP00000503080.1:n.*507A>C
ENST00000678904.1:n.2835A>C
ENST00000678910.1:c.*791A>C ENSP00000503654.1:n.*791A>C
ENST00000678925.1:c.*791A>C ENSP00000503699.1:n.*791A>C
ENST00000678964.1:c.*1522A>C ENSP00000503385.1:n.*1522A>C
ENST00000679289.1:c.*2060A>C ENSP00000504039.1:n.*2060A>C
ENST00000356245.7:c.*1055A>C ENSP00000348578.3:n.*1055A>C
ENST00000394123.7:c.*1055A>C ENSP00000377681.3:n.*1055A>C
ENST00000520177.5:c.*1996A>C ENSP00000427810.1:n.*1996A>C
NM_005754.2:c.*1055A>C NP_005745.1:n.*1055A>C
NM_198395.1:c.*1055A>C NP_938405.1:n.*1055A>C
XM_006714749.2:c.*1055A>C XP_006714812.1:n.*1055A>C
XM_006714750.2:c.*1055A>C XP_006714813.1:n.*1055A>C
NM_005754.3:c.*1055A>C MANE Select NP_005745.1:n.*1055A>C
NM_198395.2:c.*1055A>C NP_938405.1:n.*1055A>C