Canonical Allele Identifier: CA650907177

Gene: G3BP1

Linked Data

• COSMIC: COSN26649558

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151805165G>T , CM000667.2:g.151805165G>T	GRCh38
NC_000005.9:g.151184726G>T , CM000667.1:g.151184726G>T	GRCh37
NC_000005.8:g.151164919G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356245.8:c.*1074G>T MANE Select	ENSP00000348578.3:n.*1074G>T
ENST00000520177.6:c.*1261G>T	ENSP00000427810.2:n.*1261G>T
ENST00000676634.1:n.846G>T
ENST00000676644.1:c.*2452G>T	ENSP00000504249.1:n.*2452G>T
ENST00000676715.1:c.982G>T
ENST00000676734.1:c.562+719G>T	ENSP00000504327.1:n.562+719G>T
ENST00000676878.1:c.562+719G>T	ENSP00000504118.1:n.562+719G>T
ENST00000676899.1:c.870G>T
ENST00000676911.1:n.844G>T
ENST00000676978.1:c.*831G>T	ENSP00000503939.1:n.*831G>T
ENST00000677323.1:c.*1074G>T	ENSP00000502880.1:n.*1074G>T
ENST00000677381.1:c.*2015G>T	ENSP00000504403.1:n.*2015G>T
ENST00000677493.1:c.*1550G>T	ENSP00000504786.1:n.*1550G>T
ENST00000677687.1:c.133-326G>T	ENSP00000504281.1:n.133-326G>T
ENST00000677757.1:n.4325G>T
ENST00000677923.1:c.*1513G>T	ENSP00000504573.1:n.*1513G>T
ENST00000678295.1:c.1079G>T	ENSP00000503775.1:n.1079G>T
ENST00000678646.1:c.*1074G>T	ENSP00000504525.1:n.*1074G>T
ENST00000678657.1:c.1003G>T	ENSP00000504393.1:n.1003G>T
ENST00000678854.1:c.*526G>T	ENSP00000503080.1:n.*526G>T
ENST00000678904.1:n.2854G>T
ENST00000678910.1:c.*810G>T	ENSP00000503654.1:n.*810G>T
ENST00000678925.1:c.*810G>T	ENSP00000503699.1:n.*810G>T
ENST00000678964.1:c.*1541G>T	ENSP00000503385.1:n.*1541G>T
ENST00000679289.1:c.*2079G>T	ENSP00000504039.1:n.*2079G>T
ENST00000356245.7:c.*1074G>T	ENSP00000348578.3:n.*1074G>T
ENST00000394123.7:c.*1074G>T	ENSP00000377681.3:n.*1074G>T
ENST00000520177.5:c.*2015G>T	ENSP00000427810.1:n.*2015G>T
NM_005754.2:c.*1074G>T	NP_005745.1:n.*1074G>T
NM_198395.1:c.*1074G>T	NP_938405.1:n.*1074G>T
XM_006714749.2:c.*1074G>T	XP_006714812.1:n.*1074G>T
XM_006714750.2:c.*1074G>T	XP_006714813.1:n.*1074G>T
NM_005754.3:c.*1074G>T MANE Select	NP_005745.1:n.*1074G>T
NM_198395.2:c.*1074G>T	NP_938405.1:n.*1074G>T