Canonical Allele Identifier: CA346366719

Gene: SOS1

Linked Data

• MyVariant Identifiers: chr2:g.39250366A>C (hg19) ; chr2:g.39023225A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39023225A>C , CM000664.2:g.39023225A>C	GRCh38
NC_000002.11:g.39250366A>C , CM000664.1:g.39250366A>C	GRCh37
NC_000002.10:g.39103870A>C	NCBI36
NG_007530.1:g.102239T>G , LRG_754:g.102239T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000472480.2:n.1083T>G
ENST00000685279.1:c.-31T>G	ENSP00000509424.1:n.-31T>G
ENST00000688043.1:n.1424T>G
ENST00000689668.1:n.1210T>G
ENST00000690679.1:c.1390T>G
ENST00000690876.1:c.1092T>G	ENSP00000508955.1:p.Ser364Arg
ENST00000691229.1:c.1092T>G	ENSP00000510437.1:p.Ser364Arg
ENST00000692089.1:c.1092T>G	ENSP00000508626.1:p.Ser364Arg
ENST00000692620.1:c.-31T>G	ENSP00000509311.1:n.-31T>G
ENST00000402219.8:c.1203T>G MANE Select	ENSP00000384675.2:p.Ser401Arg
ENST00000395038.6:c.1203T>G	ENSP00000378479.2:p.Ser401Arg
ENST00000402219.6:c.1203T>G	ENSP00000384675.2:p.Ser401Arg
ENST00000426016.5:c.1203T>G	ENSP00000387784.1:p.Ser401Arg
ENST00000472480.1:n.47T>G
NM_005633.3:c.1203T>G , LRG_754t1:c.1203T>G	NP_005624.2:p.Ser401Arg
XM_005264515.3:c.1203T>G	XP_005264572.1:p.Ser401Arg
XM_011533060.1:c.1296T>G	XP_011531362.1:p.Ser432Arg
XM_011533061.1:c.1296T>G	XP_011531363.1:p.Ser432Arg
XM_011533062.1:c.1182T>G	XP_011531364.1:p.Ser394Arg
XM_011533063.1:c.1179T>G	XP_011531365.1:p.Ser393Arg
XM_011533064.1:c.1032T>G	XP_011531366.1:p.Ser344Arg
XM_011533065.1:c.1296T>G	XP_011531367.1:p.Ser432Arg
XM_011533066.1:c.138T>G	XP_011531368.1:p.Ser46Arg
XM_005264515.4:c.1203T>G	XP_005264572.1:p.Ser401Arg
XM_011533062.2:c.1182T>G	XP_011531364.1:p.Ser394Arg
XM_011533064.2:c.1032T>G	XP_011531366.1:p.Ser344Arg
NM_001382394.1:c.1182T>G	NP_001369323.1:p.Ser394Arg
NM_001382395.1:c.1203T>G	NP_001369324.1:p.Ser401Arg
NM_005633.4:c.1203T>G MANE Select	NP_005624.2:p.Ser401Arg