Canonical Allele Identifier: CA1591557023
Gene: G3BP1 HGNC NCBI

Linked Data

dbSNP Id: rs1762920271

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151805095T>A , CM000667.2:g.151805095T>A GRCh38
NC_000005.9:g.151184656T>A , CM000667.1:g.151184656T>A GRCh37
NC_000005.8:g.151164849T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356245.8:c.*1004T>A MANE Select ENSP00000348578.3:n.*1004T>A
ENST00000520177.6:c.*1191T>A ENSP00000427810.2:n.*1191T>A
ENST00000676634.1:n.776T>A
ENST00000676644.1:c.*2382T>A ENSP00000504249.1:n.*2382T>A
ENST00000676715.1:c.912T>A
ENST00000676734.1:c.562+649T>A ENSP00000504327.1:n.562+649T>A
ENST00000676878.1:c.562+649T>A ENSP00000504118.1:n.562+649T>A
ENST00000676899.1:c.800T>A
ENST00000676911.1:n.774T>A
ENST00000676978.1:c.*761T>A ENSP00000503939.1:n.*761T>A
ENST00000677323.1:c.*1004T>A ENSP00000502880.1:n.*1004T>A
ENST00000677381.1:c.*1945T>A ENSP00000504403.1:n.*1945T>A
ENST00000677493.1:c.*1480T>A ENSP00000504786.1:n.*1480T>A
ENST00000677687.1:c.133-396T>A ENSP00000504281.1:n.133-396T>A
ENST00000677757.1:n.4255T>A
ENST00000677923.1:c.*1443T>A ENSP00000504573.1:n.*1443T>A
ENST00000678295.1:c.1009T>A ENSP00000503775.1:n.1009T>A
ENST00000678646.1:c.*1004T>A ENSP00000504525.1:n.*1004T>A
ENST00000678657.1:c.933T>A ENSP00000504393.1:n.933T>A
ENST00000678854.1:c.*456T>A ENSP00000503080.1:n.*456T>A
ENST00000678904.1:n.2784T>A
ENST00000678910.1:c.*740T>A ENSP00000503654.1:n.*740T>A
ENST00000678925.1:c.*740T>A ENSP00000503699.1:n.*740T>A
ENST00000678964.1:c.*1471T>A ENSP00000503385.1:n.*1471T>A
ENST00000679289.1:c.*2009T>A ENSP00000504039.1:n.*2009T>A
ENST00000356245.7:c.*1004T>A ENSP00000348578.3:n.*1004T>A
ENST00000394123.7:c.*1004T>A ENSP00000377681.3:n.*1004T>A
ENST00000520177.5:c.*1945T>A ENSP00000427810.1:n.*1945T>A
NM_005754.2:c.*1004T>A NP_005745.1:n.*1004T>A
NM_198395.1:c.*1004T>A NP_938405.1:n.*1004T>A
XM_006714749.2:c.*1004T>A XP_006714812.1:n.*1004T>A
XM_006714750.2:c.*1004T>A XP_006714813.1:n.*1004T>A
NM_005754.3:c.*1004T>A MANE Select NP_005745.1:n.*1004T>A
NM_198395.2:c.*1004T>A NP_938405.1:n.*1004T>A