Canonical Allele Identifier: CA346373000

Gene: SOS1

Linked Data

• MyVariant Identifiers: chr2:g.39281799A>C (hg19) ; chr2:g.39054658A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39054658A>C , CM000664.2:g.39054658A>C	GRCh38
NC_000002.11:g.39281799A>C , CM000664.1:g.39281799A>C	GRCh37
NC_000002.10:g.39135303A>C	NCBI36
NG_007530.1:g.70806T>G , LRG_754:g.70806T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461545.2:n.703T>G
ENST00000685782.1:n.1514T>G
ENST00000688189.1:n.441T>G
ENST00000689668.1:n.683T>G
ENST00000690679.1:c.776T>G
ENST00000690876.1:c.676T>G	ENSP00000508955.1:p.Phe226Val
ENST00000691229.1:c.676T>G	ENSP00000510437.1:p.Phe226Val
ENST00000692089.1:c.676T>G	ENSP00000508626.1:p.Phe226Val
ENST00000402219.8:c.676T>G MANE Select	ENSP00000384675.2:p.Phe226Val
ENST00000395038.6:c.676T>G	ENSP00000378479.2:p.Phe226Val
ENST00000402219.6:c.676T>G	ENSP00000384675.2:p.Phe226Val
ENST00000426016.5:c.676T>G	ENSP00000387784.1:p.Phe226Val
NM_005633.3:c.676T>G , LRG_754t1:c.676T>G	NP_005624.2:p.Phe226Val
XM_005264515.3:c.676T>G	XP_005264572.1:p.Phe226Val
XM_011533060.1:c.769T>G	XP_011531362.1:p.Phe257Val
XM_011533061.1:c.769T>G	XP_011531363.1:p.Phe257Val
XM_011533062.1:c.655T>G	XP_011531364.1:p.Phe219Val
XM_011533063.1:c.652T>G	XP_011531365.1:p.Phe218Val
XM_011533064.1:c.505T>G	XP_011531366.1:p.Phe169Val
XM_011533065.1:c.769T>G	XP_011531367.1:p.Phe257Val
XM_005264515.4:c.676T>G	XP_005264572.1:p.Phe226Val
XM_011533062.2:c.655T>G	XP_011531364.1:p.Phe219Val
XM_011533064.2:c.505T>G	XP_011531366.1:p.Phe169Val
NM_001382394.1:c.655T>G	NP_001369323.1:p.Phe219Val
NM_001382395.1:c.676T>G	NP_001369324.1:p.Phe226Val
NM_005633.4:c.676T>G MANE Select	NP_005624.2:p.Phe226Val