Canonical Allele Identifier: CA346366706

Gene: SOS1

Linked Data

• MyVariant Identifiers: chr2:g.39250361G>C (hg19) ; chr2:g.39023220G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39023220G>C , CM000664.2:g.39023220G>C	GRCh38
NC_000002.11:g.39250361G>C , CM000664.1:g.39250361G>C	GRCh37
NC_000002.10:g.39103865G>C	NCBI36
NG_007530.1:g.102244C>G , LRG_754:g.102244C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000472480.2:n.1088C>G
ENST00000685279.1:c.-26C>G	ENSP00000509424.1:n.-26C>G
ENST00000688043.1:n.1429C>G
ENST00000689668.1:n.1215C>G
ENST00000690679.1:c.1395C>G
ENST00000690876.1:c.1097C>G	ENSP00000508955.1:p.Ser366Cys
ENST00000691229.1:c.1097C>G	ENSP00000510437.1:p.Ser366Cys
ENST00000692089.1:c.1097C>G	ENSP00000508626.1:p.Ser366Cys
ENST00000692620.1:c.-26C>G	ENSP00000509311.1:n.-26C>G
ENST00000402219.8:c.1208C>G MANE Select	ENSP00000384675.2:p.Ser403Cys
ENST00000395038.6:c.1208C>G	ENSP00000378479.2:p.Ser403Cys
ENST00000402219.6:c.1208C>G	ENSP00000384675.2:p.Ser403Cys
ENST00000426016.5:c.1208C>G	ENSP00000387784.1:p.Ser403Cys
ENST00000472480.1:n.52C>G
NM_005633.3:c.1208C>G , LRG_754t1:c.1208C>G	NP_005624.2:p.Ser403Cys
XM_005264515.3:c.1208C>G	XP_005264572.1:p.Ser403Cys
XM_011533060.1:c.1301C>G	XP_011531362.1:p.Ser434Cys
XM_011533061.1:c.1301C>G	XP_011531363.1:p.Ser434Cys
XM_011533062.1:c.1187C>G	XP_011531364.1:p.Ser396Cys
XM_011533063.1:c.1184C>G	XP_011531365.1:p.Ser395Cys
XM_011533064.1:c.1037C>G	XP_011531366.1:p.Ser346Cys
XM_011533065.1:c.1301C>G	XP_011531367.1:p.Ser434Cys
XM_011533066.1:c.143C>G	XP_011531368.1:p.Ser48Cys
XM_005264515.4:c.1208C>G	XP_005264572.1:p.Ser403Cys
XM_011533062.2:c.1187C>G	XP_011531364.1:p.Ser396Cys
XM_011533064.2:c.1037C>G	XP_011531366.1:p.Ser346Cys
NM_001382394.1:c.1187C>G	NP_001369323.1:p.Ser396Cys
NM_001382395.1:c.1208C>G	NP_001369324.1:p.Ser403Cys
NM_005633.4:c.1208C>G MANE Select	NP_005624.2:p.Ser403Cys