Canonical Allele Identifier: CA129996105

Gene: G3BP1

Linked Data

• dbSNP Id: rs756414791
• MyVariant Identifiers: chr5:g.151184630T>G (hg19) ; chr5:g.151805069T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151805069T>G , CM000667.2:g.151805069T>G	GRCh38
NC_000005.9:g.151184630T>G , CM000667.1:g.151184630T>G	GRCh37
NC_000005.8:g.151164823T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356245.8:c.*978T>G MANE Select	ENSP00000348578.3:n.*978T>G
ENST00000520177.6:c.*1165T>G	ENSP00000427810.2:n.*1165T>G
ENST00000676634.1:n.750T>G
ENST00000676644.1:c.*2356T>G	ENSP00000504249.1:n.*2356T>G
ENST00000676715.1:c.886T>G
ENST00000676734.1:c.562+623T>G	ENSP00000504327.1:n.562+623T>G
ENST00000676878.1:c.562+623T>G	ENSP00000504118.1:n.562+623T>G
ENST00000676899.1:c.774T>G
ENST00000676911.1:n.748T>G
ENST00000676978.1:c.*735T>G	ENSP00000503939.1:n.*735T>G
ENST00000677323.1:c.*978T>G	ENSP00000502880.1:n.*978T>G
ENST00000677381.1:c.*1919T>G	ENSP00000504403.1:n.*1919T>G
ENST00000677493.1:c.*1454T>G	ENSP00000504786.1:n.*1454T>G
ENST00000677687.1:c.133-422T>G	ENSP00000504281.1:n.133-422T>G
ENST00000677757.1:n.4229T>G
ENST00000677923.1:c.*1417T>G	ENSP00000504573.1:n.*1417T>G
ENST00000678295.1:c.983T>G	ENSP00000503775.1:n.983T>G
ENST00000678646.1:c.*978T>G	ENSP00000504525.1:n.*978T>G
ENST00000678657.1:c.907T>G	ENSP00000504393.1:n.907T>G
ENST00000678854.1:c.*430T>G	ENSP00000503080.1:n.*430T>G
ENST00000678904.1:n.2758T>G
ENST00000678910.1:c.*714T>G	ENSP00000503654.1:n.*714T>G
ENST00000678925.1:c.*714T>G	ENSP00000503699.1:n.*714T>G
ENST00000678964.1:c.*1445T>G	ENSP00000503385.1:n.*1445T>G
ENST00000679289.1:c.*1983T>G	ENSP00000504039.1:n.*1983T>G
ENST00000356245.7:c.*978T>G	ENSP00000348578.3:n.*978T>G
ENST00000394123.7:c.*978T>G	ENSP00000377681.3:n.*978T>G
ENST00000520177.5:c.*1919T>G	ENSP00000427810.1:n.*1919T>G
NM_005754.2:c.*978T>G	NP_005745.1:n.*978T>G
NM_198395.1:c.*978T>G	NP_938405.1:n.*978T>G
XM_006714749.2:c.*978T>G	XP_006714812.1:n.*978T>G
XM_006714750.2:c.*978T>G	XP_006714813.1:n.*978T>G
NM_005754.3:c.*978T>G MANE Select	NP_005745.1:n.*978T>G
NM_198395.2:c.*978T>G	NP_938405.1:n.*978T>G