Canonical Allele Identifier: CA346367775

Gene: SOS1

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39051248C>G , CM000664.2:g.39051248C>G	GRCh38
NC_000002.11:g.39278389C>G , CM000664.1:g.39278389C>G	GRCh37
NC_000002.10:g.39131893C>G	NCBI36
NG_007530.1:g.74216G>C , LRG_754:g.74216G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461545.2:n.787G>C
ENST00000472480.2:n.640G>C
ENST00000685782.1:n.1598G>C
ENST00000689668.1:n.767G>C
ENST00000690679.1:c.860G>C
ENST00000690876.1:c.760G>C	ENSP00000508955.1:p.Glu254Gln
ENST00000691229.1:c.760G>C	ENSP00000510437.1:p.Glu254Gln
ENST00000692089.1:c.760G>C	ENSP00000508626.1:p.Glu254Gln
ENST00000402219.8:c.760G>C MANE Select	ENSP00000384675.2:p.Glu254Gln
ENST00000395038.6:c.760G>C	ENSP00000378479.2:p.Glu254Gln
ENST00000402219.6:c.760G>C	ENSP00000384675.2:p.Glu254Gln
ENST00000426016.5:c.760G>C	ENSP00000387784.1:p.Glu254Gln
ENST00000461545.1:n.110G>C
NM_005633.3:c.760G>C , LRG_754t1:c.760G>C	NP_005624.2:p.Glu254Gln
XM_005264515.3:c.760G>C	XP_005264572.1:p.Glu254Gln
XM_011533060.1:c.853G>C	XP_011531362.1:p.Glu285Gln
XM_011533061.1:c.853G>C	XP_011531363.1:p.Glu285Gln
XM_011533062.1:c.739G>C	XP_011531364.1:p.Glu247Gln
XM_011533063.1:c.736G>C	XP_011531365.1:p.Glu246Gln
XM_011533064.1:c.589G>C	XP_011531366.1:p.Glu197Gln
XM_011533065.1:c.853G>C	XP_011531367.1:p.Glu285Gln
XM_005264515.4:c.760G>C	XP_005264572.1:p.Glu254Gln
XM_011533062.2:c.739G>C	XP_011531364.1:p.Glu247Gln
XM_011533064.2:c.589G>C	XP_011531366.1:p.Glu197Gln
NM_001382394.1:c.739G>C	NP_001369323.1:p.Glu247Gln
NM_001382395.1:c.760G>C	NP_001369324.1:p.Glu254Gln
NM_005633.4:c.760G>C MANE Select	NP_005624.2:p.Glu254Gln