Canonical Allele Identifier: CA2710197722

Gene: G3BP1

Linked Data

• dbSNP Id: rs2113256666

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151805118A>G , CM000667.2:g.151805118A>G	GRCh38
NC_000005.9:g.151184679A>G , CM000667.1:g.151184679A>G	GRCh37
NC_000005.8:g.151164872A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356245.8:c.*1027A>G MANE Select	ENSP00000348578.3:n.*1027A>G
ENST00000520177.6:c.*1214A>G	ENSP00000427810.2:n.*1214A>G
ENST00000676634.1:n.799A>G
ENST00000676644.1:c.*2405A>G	ENSP00000504249.1:n.*2405A>G
ENST00000676715.1:c.935A>G
ENST00000676734.1:c.562+672A>G	ENSP00000504327.1:n.562+672A>G
ENST00000676878.1:c.562+672A>G	ENSP00000504118.1:n.562+672A>G
ENST00000676899.1:c.823A>G
ENST00000676911.1:n.797A>G
ENST00000676978.1:c.*784A>G	ENSP00000503939.1:n.*784A>G
ENST00000677323.1:c.*1027A>G	ENSP00000502880.1:n.*1027A>G
ENST00000677381.1:c.*1968A>G	ENSP00000504403.1:n.*1968A>G
ENST00000677493.1:c.*1503A>G	ENSP00000504786.1:n.*1503A>G
ENST00000677687.1:c.133-373A>G	ENSP00000504281.1:n.133-373A>G
ENST00000677757.1:n.4278A>G
ENST00000677923.1:c.*1466A>G	ENSP00000504573.1:n.*1466A>G
ENST00000678295.1:c.1032A>G	ENSP00000503775.1:n.1032A>G
ENST00000678646.1:c.*1027A>G	ENSP00000504525.1:n.*1027A>G
ENST00000678657.1:c.956A>G	ENSP00000504393.1:n.956A>G
ENST00000678854.1:c.*479A>G	ENSP00000503080.1:n.*479A>G
ENST00000678904.1:n.2807A>G
ENST00000678910.1:c.*763A>G	ENSP00000503654.1:n.*763A>G
ENST00000678925.1:c.*763A>G	ENSP00000503699.1:n.*763A>G
ENST00000678964.1:c.*1494A>G	ENSP00000503385.1:n.*1494A>G
ENST00000679289.1:c.*2032A>G	ENSP00000504039.1:n.*2032A>G
ENST00000356245.7:c.*1027A>G	ENSP00000348578.3:n.*1027A>G
ENST00000394123.7:c.*1027A>G	ENSP00000377681.3:n.*1027A>G
ENST00000520177.5:c.*1968A>G	ENSP00000427810.1:n.*1968A>G
NM_005754.2:c.*1027A>G	NP_005745.1:n.*1027A>G
NM_198395.1:c.*1027A>G	NP_938405.1:n.*1027A>G
XM_006714749.2:c.*1027A>G	XP_006714812.1:n.*1027A>G
XM_006714750.2:c.*1027A>G	XP_006714813.1:n.*1027A>G
NM_005754.3:c.*1027A>G MANE Select	NP_005745.1:n.*1027A>G
NM_198395.2:c.*1027A>G	NP_938405.1:n.*1027A>G