Canonical Allele Identifier: CA2768928239

Gene: G3BP1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151805014T>C , CM000667.2:g.151805014T>C	GRCh38
NC_000005.9:g.151184575T>C , CM000667.1:g.151184575T>C	GRCh37
NC_000005.8:g.151164768T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356245.8:c.*923T>C MANE Select	ENSP00000348578.3:n.*923T>C
ENST00000520177.6:c.*1110T>C	ENSP00000427810.2:n.*1110T>C
ENST00000676634.1:n.695T>C
ENST00000676644.1:c.*2301T>C	ENSP00000504249.1:n.*2301T>C
ENST00000676715.1:c.831T>C
ENST00000676734.1:c.562+568T>C	ENSP00000504327.1:n.562+568T>C
ENST00000676878.1:c.562+568T>C	ENSP00000504118.1:n.562+568T>C
ENST00000676899.1:c.719T>C
ENST00000676911.1:n.693T>C
ENST00000676978.1:c.*680T>C	ENSP00000503939.1:n.*680T>C
ENST00000677323.1:c.*923T>C	ENSP00000502880.1:n.*923T>C
ENST00000677381.1:c.*1864T>C	ENSP00000504403.1:n.*1864T>C
ENST00000677493.1:c.*1399T>C	ENSP00000504786.1:n.*1399T>C
ENST00000677687.1:c.133-477T>C	ENSP00000504281.1:n.133-477T>C
ENST00000677757.1:n.4174T>C
ENST00000677923.1:c.*1362T>C	ENSP00000504573.1:n.*1362T>C
ENST00000678295.1:c.928T>C	ENSP00000503775.1:n.928T>C
ENST00000678646.1:c.*923T>C	ENSP00000504525.1:n.*923T>C
ENST00000678657.1:c.852T>C	ENSP00000504393.1:n.852T>C
ENST00000678854.1:c.*375T>C	ENSP00000503080.1:n.*375T>C
ENST00000678904.1:n.2703T>C
ENST00000678910.1:c.*659T>C	ENSP00000503654.1:n.*659T>C
ENST00000678925.1:c.*659T>C	ENSP00000503699.1:n.*659T>C
ENST00000678964.1:c.*1390T>C	ENSP00000503385.1:n.*1390T>C
ENST00000679289.1:c.*1928T>C	ENSP00000504039.1:n.*1928T>C
ENST00000356245.7:c.*923T>C	ENSP00000348578.3:n.*923T>C
ENST00000394123.7:c.*923T>C	ENSP00000377681.3:n.*923T>C
ENST00000520177.5:c.*1864T>C	ENSP00000427810.1:n.*1864T>C
NM_005754.2:c.*923T>C	NP_005745.1:n.*923T>C
NM_198395.1:c.*923T>C	NP_938405.1:n.*923T>C
XM_006714749.2:c.*923T>C	XP_006714812.1:n.*923T>C
XM_006714750.2:c.*923T>C	XP_006714813.1:n.*923T>C
NM_005754.3:c.*923T>C MANE Select	NP_005745.1:n.*923T>C
NM_198395.2:c.*923T>C	NP_938405.1:n.*923T>C