Canonical Allele Identifier: CA2676107732

Gene: G3BP1

Linked Data

• gnomAD v4: 5-151805206-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151805206G>T , CM000667.2:g.151805206G>T	GRCh38
NC_000005.9:g.151184767G>T , CM000667.1:g.151184767G>T	GRCh37
NC_000005.8:g.151164960G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356245.8:c.*1115G>T MANE Select	ENSP00000348578.3:n.*1115G>T
ENST00000520177.6:c.*1302G>T	ENSP00000427810.2:n.*1302G>T
ENST00000676634.1:n.887G>T
ENST00000676644.1:c.*2493G>T	ENSP00000504249.1:n.*2493G>T
ENST00000676715.1:c.1023G>T
ENST00000676734.1:c.562+760G>T	ENSP00000504327.1:n.562+760G>T
ENST00000676878.1:c.562+760G>T	ENSP00000504118.1:n.562+760G>T
ENST00000676899.1:c.911G>T
ENST00000676911.1:n.885G>T
ENST00000676978.1:c.*872G>T	ENSP00000503939.1:n.*872G>T
ENST00000677323.1:c.*1115G>T	ENSP00000502880.1:n.*1115G>T
ENST00000677381.1:c.*2056G>T	ENSP00000504403.1:n.*2056G>T
ENST00000677493.1:c.*1591G>T	ENSP00000504786.1:n.*1591G>T
ENST00000677687.1:c.133-285G>T	ENSP00000504281.1:n.133-285G>T
ENST00000677757.1:n.4366G>T
ENST00000677923.1:c.*1554G>T	ENSP00000504573.1:n.*1554G>T
ENST00000678295.1:c.1120G>T	ENSP00000503775.1:n.1120G>T
ENST00000678646.1:c.*1115G>T	ENSP00000504525.1:n.*1115G>T
ENST00000678657.1:c.1044G>T	ENSP00000504393.1:n.1044G>T
ENST00000678854.1:c.*567G>T	ENSP00000503080.1:n.*567G>T
ENST00000678904.1:n.2895G>T
ENST00000678910.1:c.*851G>T	ENSP00000503654.1:n.*851G>T
ENST00000678925.1:c.*851G>T	ENSP00000503699.1:n.*851G>T
ENST00000678964.1:c.*1582G>T	ENSP00000503385.1:n.*1582G>T
ENST00000679289.1:c.*2120G>T	ENSP00000504039.1:n.*2120G>T
ENST00000356245.7:c.*1115G>T	ENSP00000348578.3:n.*1115G>T
ENST00000394123.7:c.*1115G>T	ENSP00000377681.3:n.*1115G>T
ENST00000520177.5:c.*2056G>T	ENSP00000427810.1:n.*2056G>T
NM_005754.2:c.*1115G>T	NP_005745.1:n.*1115G>T
NM_198395.1:c.*1115G>T	NP_938405.1:n.*1115G>T
XM_006714749.2:c.*1115G>T	XP_006714812.1:n.*1115G>T
XM_006714750.2:c.*1115G>T	XP_006714813.1:n.*1115G>T
NM_005754.3:c.*1115G>T MANE Select	NP_005745.1:n.*1115G>T
NM_198395.2:c.*1115G>T	NP_938405.1:n.*1115G>T