Canonical Allele Identifier: CA346372926

Gene: SOS1

Linked Data

• MyVariant Identifiers: chr2:g.39281766A>T (hg19) ; chr2:g.39054625A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39054625A>T , CM000664.2:g.39054625A>T	GRCh38
NC_000002.11:g.39281766A>T , CM000664.1:g.39281766A>T	GRCh37
NC_000002.10:g.39135270A>T	NCBI36
NG_007530.1:g.70839T>A , LRG_754:g.70839T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461545.2:n.736T>A
ENST00000685782.1:n.1547T>A
ENST00000688189.1:n.474T>A
ENST00000689668.1:n.716T>A
ENST00000690679.1:c.809T>A
ENST00000690876.1:c.709T>A	ENSP00000508955.1:p.Phe237Ile
ENST00000691229.1:c.709T>A	ENSP00000510437.1:p.Phe237Ile
ENST00000692089.1:c.709T>A	ENSP00000508626.1:p.Phe237Ile
ENST00000402219.8:c.709T>A MANE Select	ENSP00000384675.2:p.Phe237Ile
ENST00000395038.6:c.709T>A	ENSP00000378479.2:p.Phe237Ile
ENST00000402219.6:c.709T>A	ENSP00000384675.2:p.Phe237Ile
ENST00000426016.5:c.709T>A	ENSP00000387784.1:p.Phe237Ile
NM_005633.3:c.709T>A , LRG_754t1:c.709T>A	NP_005624.2:p.Phe237Ile
XM_005264515.3:c.709T>A	XP_005264572.1:p.Phe237Ile
XM_011533060.1:c.802T>A	XP_011531362.1:p.Phe268Ile
XM_011533061.1:c.802T>A	XP_011531363.1:p.Phe268Ile
XM_011533062.1:c.688T>A	XP_011531364.1:p.Phe230Ile
XM_011533063.1:c.685T>A	XP_011531365.1:p.Phe229Ile
XM_011533064.1:c.538T>A	XP_011531366.1:p.Phe180Ile
XM_011533065.1:c.802T>A	XP_011531367.1:p.Phe268Ile
XM_005264515.4:c.709T>A	XP_005264572.1:p.Phe237Ile
XM_011533062.2:c.688T>A	XP_011531364.1:p.Phe230Ile
XM_011533064.2:c.538T>A	XP_011531366.1:p.Phe180Ile
NM_001382394.1:c.688T>A	NP_001369323.1:p.Phe230Ile
NM_001382395.1:c.709T>A	NP_001369324.1:p.Phe237Ile
NM_005633.4:c.709T>A MANE Select	NP_005624.2:p.Phe237Ile