Canonical Allele Identifier: CA1591556997

Gene: G3BP1

Linked Data

• dbSNP Id: rs1762918598

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151805044A>C , CM000667.2:g.151805044A>C	GRCh38
NC_000005.9:g.151184605A>C , CM000667.1:g.151184605A>C	GRCh37
NC_000005.8:g.151164798A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356245.8:c.*953A>C MANE Select	ENSP00000348578.3:n.*953A>C
ENST00000520177.6:c.*1140A>C	ENSP00000427810.2:n.*1140A>C
ENST00000676634.1:n.725A>C
ENST00000676644.1:c.*2331A>C	ENSP00000504249.1:n.*2331A>C
ENST00000676715.1:c.861A>C
ENST00000676734.1:c.562+598A>C	ENSP00000504327.1:n.562+598A>C
ENST00000676878.1:c.562+598A>C	ENSP00000504118.1:n.562+598A>C
ENST00000676899.1:c.749A>C
ENST00000676911.1:n.723A>C
ENST00000676978.1:c.*710A>C	ENSP00000503939.1:n.*710A>C
ENST00000677323.1:c.*953A>C	ENSP00000502880.1:n.*953A>C
ENST00000677381.1:c.*1894A>C	ENSP00000504403.1:n.*1894A>C
ENST00000677493.1:c.*1429A>C	ENSP00000504786.1:n.*1429A>C
ENST00000677687.1:c.133-447A>C	ENSP00000504281.1:n.133-447A>C
ENST00000677757.1:n.4204A>C
ENST00000677923.1:c.*1392A>C	ENSP00000504573.1:n.*1392A>C
ENST00000678295.1:c.958A>C	ENSP00000503775.1:n.958A>C
ENST00000678646.1:c.*953A>C	ENSP00000504525.1:n.*953A>C
ENST00000678657.1:c.882A>C	ENSP00000504393.1:n.882A>C
ENST00000678854.1:c.*405A>C	ENSP00000503080.1:n.*405A>C
ENST00000678904.1:n.2733A>C
ENST00000678910.1:c.*689A>C	ENSP00000503654.1:n.*689A>C
ENST00000678925.1:c.*689A>C	ENSP00000503699.1:n.*689A>C
ENST00000678964.1:c.*1420A>C	ENSP00000503385.1:n.*1420A>C
ENST00000679289.1:c.*1958A>C	ENSP00000504039.1:n.*1958A>C
ENST00000356245.7:c.*953A>C	ENSP00000348578.3:n.*953A>C
ENST00000394123.7:c.*953A>C	ENSP00000377681.3:n.*953A>C
ENST00000520177.5:c.*1894A>C	ENSP00000427810.1:n.*1894A>C
NM_005754.2:c.*953A>C	NP_005745.1:n.*953A>C
NM_198395.1:c.*953A>C	NP_938405.1:n.*953A>C
XM_006714749.2:c.*953A>C	XP_006714812.1:n.*953A>C
XM_006714750.2:c.*953A>C	XP_006714813.1:n.*953A>C
NM_005754.3:c.*953A>C MANE Select	NP_005745.1:n.*953A>C
NM_198395.2:c.*953A>C	NP_938405.1:n.*953A>C