Canonical Allele Identifier: CA129996185

Gene: G3BP1

Linked Data

• dbSNP Id: rs988713008
• gnomAD v2: 5-151184755-C-G
• gnomAD v3: 5-151805194-C-G
• gnomAD v4: 5-151805194-C-G
• MyVariant Identifiers: chr5:g.151184755C>G (hg19) ; chr5:g.151805194C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151805194C>G , CM000667.2:g.151805194C>G	GRCh38
NC_000005.9:g.151184755C>G , CM000667.1:g.151184755C>G	GRCh37
NC_000005.8:g.151164948C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356245.8:c.*1103C>G MANE Select	ENSP00000348578.3:n.*1103C>G
ENST00000520177.6:c.*1290C>G	ENSP00000427810.2:n.*1290C>G
ENST00000676634.1:n.875C>G
ENST00000676644.1:c.*2481C>G	ENSP00000504249.1:n.*2481C>G
ENST00000676715.1:c.1011C>G
ENST00000676734.1:c.562+748C>G	ENSP00000504327.1:n.562+748C>G
ENST00000676878.1:c.562+748C>G	ENSP00000504118.1:n.562+748C>G
ENST00000676899.1:c.899C>G
ENST00000676911.1:n.873C>G
ENST00000676978.1:c.*860C>G	ENSP00000503939.1:n.*860C>G
ENST00000677323.1:c.*1103C>G	ENSP00000502880.1:n.*1103C>G
ENST00000677381.1:c.*2044C>G	ENSP00000504403.1:n.*2044C>G
ENST00000677493.1:c.*1579C>G	ENSP00000504786.1:n.*1579C>G
ENST00000677687.1:c.133-297C>G	ENSP00000504281.1:n.133-297C>G
ENST00000677757.1:n.4354C>G
ENST00000677923.1:c.*1542C>G	ENSP00000504573.1:n.*1542C>G
ENST00000678295.1:c.1108C>G	ENSP00000503775.1:n.1108C>G
ENST00000678646.1:c.*1103C>G	ENSP00000504525.1:n.*1103C>G
ENST00000678657.1:c.1032C>G	ENSP00000504393.1:n.1032C>G
ENST00000678854.1:c.*555C>G	ENSP00000503080.1:n.*555C>G
ENST00000678904.1:n.2883C>G
ENST00000678910.1:c.*839C>G	ENSP00000503654.1:n.*839C>G
ENST00000678925.1:c.*839C>G	ENSP00000503699.1:n.*839C>G
ENST00000678964.1:c.*1570C>G	ENSP00000503385.1:n.*1570C>G
ENST00000679289.1:c.*2108C>G	ENSP00000504039.1:n.*2108C>G
ENST00000356245.7:c.*1103C>G	ENSP00000348578.3:n.*1103C>G
ENST00000394123.7:c.*1103C>G	ENSP00000377681.3:n.*1103C>G
ENST00000520177.5:c.*2044C>G	ENSP00000427810.1:n.*2044C>G
NM_005754.2:c.*1103C>G	NP_005745.1:n.*1103C>G
NM_198395.1:c.*1103C>G	NP_938405.1:n.*1103C>G
XM_006714749.2:c.*1103C>G	XP_006714812.1:n.*1103C>G
XM_006714750.2:c.*1103C>G	XP_006714813.1:n.*1103C>G
NM_005754.3:c.*1103C>G MANE Select	NP_005745.1:n.*1103C>G
NM_198395.2:c.*1103C>G	NP_938405.1:n.*1103C>G