Canonical Allele Identifier: CA2768928236

Gene: G3BP1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151804963G>C , CM000667.2:g.151804963G>C	GRCh38
NC_000005.9:g.151184524G>C , CM000667.1:g.151184524G>C	GRCh37
NC_000005.8:g.151164717G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356245.8:c.*872G>C MANE Select	ENSP00000348578.3:n.*872G>C
ENST00000520177.6:c.*1059G>C	ENSP00000427810.2:n.*1059G>C
ENST00000676634.1:n.644G>C
ENST00000676644.1:c.*2250G>C	ENSP00000504249.1:n.*2250G>C
ENST00000676715.1:c.780G>C
ENST00000676734.1:c.562+517G>C	ENSP00000504327.1:n.562+517G>C
ENST00000676878.1:c.562+517G>C	ENSP00000504118.1:n.562+517G>C
ENST00000676899.1:c.668G>C
ENST00000676911.1:n.642G>C
ENST00000676978.1:c.*629G>C	ENSP00000503939.1:n.*629G>C
ENST00000677323.1:c.*872G>C	ENSP00000502880.1:n.*872G>C
ENST00000677381.1:c.*1813G>C	ENSP00000504403.1:n.*1813G>C
ENST00000677493.1:c.*1348G>C	ENSP00000504786.1:n.*1348G>C
ENST00000677687.1:c.133-528G>C	ENSP00000504281.1:n.133-528G>C
ENST00000677757.1:n.4123G>C
ENST00000677923.1:c.*1311G>C	ENSP00000504573.1:n.*1311G>C
ENST00000678295.1:c.877G>C	ENSP00000503775.1:n.877G>C
ENST00000678646.1:c.*872G>C	ENSP00000504525.1:n.*872G>C
ENST00000678657.1:c.801G>C	ENSP00000504393.1:n.801G>C
ENST00000678854.1:c.*324G>C	ENSP00000503080.1:n.*324G>C
ENST00000678904.1:n.2652G>C
ENST00000678910.1:c.*608G>C	ENSP00000503654.1:n.*608G>C
ENST00000678925.1:c.*608G>C	ENSP00000503699.1:n.*608G>C
ENST00000678964.1:c.*1339G>C	ENSP00000503385.1:n.*1339G>C
ENST00000679289.1:c.*1877G>C	ENSP00000504039.1:n.*1877G>C
ENST00000356245.7:c.*872G>C	ENSP00000348578.3:n.*872G>C
ENST00000394123.7:c.*872G>C	ENSP00000377681.3:n.*872G>C
ENST00000520177.5:c.*1813G>C	ENSP00000427810.1:n.*1813G>C
NM_005754.2:c.*872G>C	NP_005745.1:n.*872G>C
NM_198395.1:c.*872G>C	NP_938405.1:n.*872G>C
XM_006714749.2:c.*872G>C	XP_006714812.1:n.*872G>C
XM_006714750.2:c.*872G>C	XP_006714813.1:n.*872G>C
NM_005754.3:c.*872G>C MANE Select	NP_005745.1:n.*872G>C
NM_198395.2:c.*872G>C	NP_938405.1:n.*872G>C