Canonical Allele Identifier: CA805712367

Gene: G3BP1

Linked Data

• dbSNP Id: rs1161143858
• gnomAD v3: 5-151805068-C-T
• gnomAD v4: 5-151805068-C-T
• MyVariant Identifiers: chr5:g.151184629C>T (hg19) ; chr5:g.151805068C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151805068C>T , CM000667.2:g.151805068C>T	GRCh38
NC_000005.9:g.151184629C>T , CM000667.1:g.151184629C>T	GRCh37
NC_000005.8:g.151164822C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356245.8:c.*977C>T MANE Select	ENSP00000348578.3:n.*977C>T
ENST00000520177.6:c.*1164C>T	ENSP00000427810.2:n.*1164C>T
ENST00000676634.1:n.749C>T
ENST00000676644.1:c.*2355C>T	ENSP00000504249.1:n.*2355C>T
ENST00000676715.1:c.885C>T
ENST00000676734.1:c.562+622C>T	ENSP00000504327.1:n.562+622C>T
ENST00000676878.1:c.562+622C>T	ENSP00000504118.1:n.562+622C>T
ENST00000676899.1:c.773C>T
ENST00000676911.1:n.747C>T
ENST00000676978.1:c.*734C>T	ENSP00000503939.1:n.*734C>T
ENST00000677323.1:c.*977C>T	ENSP00000502880.1:n.*977C>T
ENST00000677381.1:c.*1918C>T	ENSP00000504403.1:n.*1918C>T
ENST00000677493.1:c.*1453C>T	ENSP00000504786.1:n.*1453C>T
ENST00000677687.1:c.133-423C>T	ENSP00000504281.1:n.133-423C>T
ENST00000677757.1:n.4228C>T
ENST00000677923.1:c.*1416C>T	ENSP00000504573.1:n.*1416C>T
ENST00000678295.1:c.982C>T	ENSP00000503775.1:n.982C>T
ENST00000678646.1:c.*977C>T	ENSP00000504525.1:n.*977C>T
ENST00000678657.1:c.906C>T	ENSP00000504393.1:n.906C>T
ENST00000678854.1:c.*429C>T	ENSP00000503080.1:n.*429C>T
ENST00000678904.1:n.2757C>T
ENST00000678910.1:c.*713C>T	ENSP00000503654.1:n.*713C>T
ENST00000678925.1:c.*713C>T	ENSP00000503699.1:n.*713C>T
ENST00000678964.1:c.*1444C>T	ENSP00000503385.1:n.*1444C>T
ENST00000679289.1:c.*1982C>T	ENSP00000504039.1:n.*1982C>T
ENST00000356245.7:c.*977C>T	ENSP00000348578.3:n.*977C>T
ENST00000394123.7:c.*977C>T	ENSP00000377681.3:n.*977C>T
ENST00000520177.5:c.*1918C>T	ENSP00000427810.1:n.*1918C>T
NM_005754.2:c.*977C>T	NP_005745.1:n.*977C>T
NM_198395.1:c.*977C>T	NP_938405.1:n.*977C>T
XM_006714749.2:c.*977C>T	XP_006714812.1:n.*977C>T
XM_006714750.2:c.*977C>T	XP_006714813.1:n.*977C>T
NM_005754.3:c.*977C>T MANE Select	NP_005745.1:n.*977C>T
NM_198395.2:c.*977C>T	NP_938405.1:n.*977C>T