Canonical Allele Identifier: CA563631026

Gene: G3BP1

Linked Data

• dbSNP Id: rs1312657942
• gnomAD v2: 5-151184753-G-A
• gnomAD v3: 5-151805192-G-A
• gnomAD v4: 5-151805192-G-A
• MyVariant Identifiers: chr5:g.151184753G>A (hg19) ; chr5:g.151805192G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151805192G>A , CM000667.2:g.151805192G>A	GRCh38
NC_000005.9:g.151184753G>A , CM000667.1:g.151184753G>A	GRCh37
NC_000005.8:g.151164946G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356245.8:c.*1101G>A MANE Select	ENSP00000348578.3:n.*1101G>A
ENST00000520177.6:c.*1288G>A	ENSP00000427810.2:n.*1288G>A
ENST00000676634.1:n.873G>A
ENST00000676644.1:c.*2479G>A	ENSP00000504249.1:n.*2479G>A
ENST00000676715.1:c.1009G>A
ENST00000676734.1:c.562+746G>A	ENSP00000504327.1:n.562+746G>A
ENST00000676878.1:c.562+746G>A	ENSP00000504118.1:n.562+746G>A
ENST00000676899.1:c.897G>A
ENST00000676911.1:n.871G>A
ENST00000676978.1:c.*858G>A	ENSP00000503939.1:n.*858G>A
ENST00000677323.1:c.*1101G>A	ENSP00000502880.1:n.*1101G>A
ENST00000677381.1:c.*2042G>A	ENSP00000504403.1:n.*2042G>A
ENST00000677493.1:c.*1577G>A	ENSP00000504786.1:n.*1577G>A
ENST00000677687.1:c.133-299G>A	ENSP00000504281.1:n.133-299G>A
ENST00000677757.1:n.4352G>A
ENST00000677923.1:c.*1540G>A	ENSP00000504573.1:n.*1540G>A
ENST00000678295.1:c.1106G>A	ENSP00000503775.1:n.1106G>A
ENST00000678646.1:c.*1101G>A	ENSP00000504525.1:n.*1101G>A
ENST00000678657.1:c.1030G>A	ENSP00000504393.1:n.1030G>A
ENST00000678854.1:c.*553G>A	ENSP00000503080.1:n.*553G>A
ENST00000678904.1:n.2881G>A
ENST00000678910.1:c.*837G>A	ENSP00000503654.1:n.*837G>A
ENST00000678925.1:c.*837G>A	ENSP00000503699.1:n.*837G>A
ENST00000678964.1:c.*1568G>A	ENSP00000503385.1:n.*1568G>A
ENST00000679289.1:c.*2106G>A	ENSP00000504039.1:n.*2106G>A
ENST00000356245.7:c.*1101G>A	ENSP00000348578.3:n.*1101G>A
ENST00000394123.7:c.*1101G>A	ENSP00000377681.3:n.*1101G>A
ENST00000520177.5:c.*2042G>A	ENSP00000427810.1:n.*2042G>A
NM_005754.2:c.*1101G>A	NP_005745.1:n.*1101G>A
NM_198395.1:c.*1101G>A	NP_938405.1:n.*1101G>A
XM_006714749.2:c.*1101G>A	XP_006714812.1:n.*1101G>A
XM_006714750.2:c.*1101G>A	XP_006714813.1:n.*1101G>A
NM_005754.3:c.*1101G>A MANE Select	NP_005745.1:n.*1101G>A
NM_198395.2:c.*1101G>A	NP_938405.1:n.*1101G>A