Canonical Allele Identifier: CA12067060
Gene: G3BP1 HGNC NCBI

Linked Data

dbSNP Id: rs1062177

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151805140C>T , CM000667.2:g.151805140C>T GRCh38
NC_000005.9:g.151184701C>T , CM000667.1:g.151184701C>T GRCh37
NC_000005.8:g.151164894C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356245.8:c.*1049C>T MANE Select ENSP00000348578.3:n.*1049C>T
ENST00000520177.6:c.*1236C>T ENSP00000427810.2:n.*1236C>T
ENST00000676634.1:n.821C>T
ENST00000676644.1:c.*2427C>T ENSP00000504249.1:n.*2427C>T
ENST00000676715.1:c.957C>T
ENST00000676734.1:c.562+694C>T ENSP00000504327.1:n.562+694C>T
ENST00000676878.1:c.562+694C>T ENSP00000504118.1:n.562+694C>T
ENST00000676899.1:c.845C>T
ENST00000676911.1:n.819C>T
ENST00000676978.1:c.*806C>T ENSP00000503939.1:n.*806C>T
ENST00000677323.1:c.*1049C>T ENSP00000502880.1:n.*1049C>T
ENST00000677381.1:c.*1990C>T ENSP00000504403.1:n.*1990C>T
ENST00000677493.1:c.*1525C>T ENSP00000504786.1:n.*1525C>T
ENST00000677687.1:c.133-351C>T ENSP00000504281.1:n.133-351C>T
ENST00000677757.1:n.4300C>T
ENST00000677923.1:c.*1488C>T ENSP00000504573.1:n.*1488C>T
ENST00000678295.1:c.1054C>T ENSP00000503775.1:n.1054C>T
ENST00000678646.1:c.*1049C>T ENSP00000504525.1:n.*1049C>T
ENST00000678657.1:c.978C>T ENSP00000504393.1:n.978C>T
ENST00000678854.1:c.*501C>T ENSP00000503080.1:n.*501C>T
ENST00000678904.1:n.2829C>T
ENST00000678910.1:c.*785C>T ENSP00000503654.1:n.*785C>T
ENST00000678925.1:c.*785C>T ENSP00000503699.1:n.*785C>T
ENST00000678964.1:c.*1516C>T ENSP00000503385.1:n.*1516C>T
ENST00000679289.1:c.*2054C>T ENSP00000504039.1:n.*2054C>T
ENST00000356245.7:c.*1049C>T ENSP00000348578.3:n.*1049C>T
ENST00000394123.7:c.*1049C>T ENSP00000377681.3:n.*1049C>T
ENST00000520177.5:c.*1990C>T ENSP00000427810.1:n.*1990C>T
NM_005754.2:c.*1049C>T NP_005745.1:n.*1049C>T
NM_198395.1:c.*1049C>T NP_938405.1:n.*1049C>T
XM_006714749.2:c.*1049C>T XP_006714812.1:n.*1049C>T
XM_006714750.2:c.*1049C>T XP_006714813.1:n.*1049C>T
NM_005754.3:c.*1049C>T MANE Select NP_005745.1:n.*1049C>T
NM_198395.2:c.*1049C>T NP_938405.1:n.*1049C>T