Canonical Allele Identifier: CA805712426

Gene: G3BP1

Linked Data

• dbSNP Id: rs1365705767
• MyVariant Identifiers: chr5:g.151184745T>C (hg19) ; chr5:g.151805184T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151805184T>C , CM000667.2:g.151805184T>C	GRCh38
NC_000005.9:g.151184745T>C , CM000667.1:g.151184745T>C	GRCh37
NC_000005.8:g.151164938T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356245.8:c.*1093T>C MANE Select	ENSP00000348578.3:n.*1093T>C
ENST00000520177.6:c.*1280T>C	ENSP00000427810.2:n.*1280T>C
ENST00000676634.1:n.865T>C
ENST00000676644.1:c.*2471T>C	ENSP00000504249.1:n.*2471T>C
ENST00000676715.1:c.1001T>C
ENST00000676734.1:c.562+738T>C	ENSP00000504327.1:n.562+738T>C
ENST00000676878.1:c.562+738T>C	ENSP00000504118.1:n.562+738T>C
ENST00000676899.1:c.889T>C
ENST00000676911.1:n.863T>C
ENST00000676978.1:c.*850T>C	ENSP00000503939.1:n.*850T>C
ENST00000677323.1:c.*1093T>C	ENSP00000502880.1:n.*1093T>C
ENST00000677381.1:c.*2034T>C	ENSP00000504403.1:n.*2034T>C
ENST00000677493.1:c.*1569T>C	ENSP00000504786.1:n.*1569T>C
ENST00000677687.1:c.133-307T>C	ENSP00000504281.1:n.133-307T>C
ENST00000677757.1:n.4344T>C
ENST00000677923.1:c.*1532T>C	ENSP00000504573.1:n.*1532T>C
ENST00000678295.1:c.1098T>C	ENSP00000503775.1:n.1098T>C
ENST00000678646.1:c.*1093T>C	ENSP00000504525.1:n.*1093T>C
ENST00000678657.1:c.1022T>C	ENSP00000504393.1:n.1022T>C
ENST00000678854.1:c.*545T>C	ENSP00000503080.1:n.*545T>C
ENST00000678904.1:n.2873T>C
ENST00000678910.1:c.*829T>C	ENSP00000503654.1:n.*829T>C
ENST00000678925.1:c.*829T>C	ENSP00000503699.1:n.*829T>C
ENST00000678964.1:c.*1560T>C	ENSP00000503385.1:n.*1560T>C
ENST00000679289.1:c.*2098T>C	ENSP00000504039.1:n.*2098T>C
ENST00000356245.7:c.*1093T>C	ENSP00000348578.3:n.*1093T>C
ENST00000394123.7:c.*1093T>C	ENSP00000377681.3:n.*1093T>C
ENST00000520177.5:c.*2034T>C	ENSP00000427810.1:n.*2034T>C
NM_005754.2:c.*1093T>C	NP_005745.1:n.*1093T>C
NM_198395.1:c.*1093T>C	NP_938405.1:n.*1093T>C
XM_006714749.2:c.*1093T>C	XP_006714812.1:n.*1093T>C
XM_006714750.2:c.*1093T>C	XP_006714813.1:n.*1093T>C
NM_005754.3:c.*1093T>C MANE Select	NP_005745.1:n.*1093T>C
NM_198395.2:c.*1093T>C	NP_938405.1:n.*1093T>C