Canonical Allele Identifier: CA346366710

Gene: SOS1

Linked Data

• MyVariant Identifiers: chr2:g.39250362A>T (hg19) ; chr2:g.39023221A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39023221A>T , CM000664.2:g.39023221A>T	GRCh38
NC_000002.11:g.39250362A>T , CM000664.1:g.39250362A>T	GRCh37
NC_000002.10:g.39103866A>T	NCBI36
NG_007530.1:g.102243T>A , LRG_754:g.102243T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000472480.2:n.1087T>A
ENST00000685279.1:c.-27T>A	ENSP00000509424.1:n.-27T>A
ENST00000688043.1:n.1428T>A
ENST00000689668.1:n.1214T>A
ENST00000690679.1:c.1394T>A
ENST00000690876.1:c.1096T>A	ENSP00000508955.1:p.Ser366Thr
ENST00000691229.1:c.1096T>A	ENSP00000510437.1:p.Ser366Thr
ENST00000692089.1:c.1096T>A	ENSP00000508626.1:p.Ser366Thr
ENST00000692620.1:c.-27T>A	ENSP00000509311.1:n.-27T>A
ENST00000402219.8:c.1207T>A MANE Select	ENSP00000384675.2:p.Ser403Thr
ENST00000395038.6:c.1207T>A	ENSP00000378479.2:p.Ser403Thr
ENST00000402219.6:c.1207T>A	ENSP00000384675.2:p.Ser403Thr
ENST00000426016.5:c.1207T>A	ENSP00000387784.1:p.Ser403Thr
ENST00000472480.1:n.51T>A
NM_005633.3:c.1207T>A , LRG_754t1:c.1207T>A	NP_005624.2:p.Ser403Thr
XM_005264515.3:c.1207T>A	XP_005264572.1:p.Ser403Thr
XM_011533060.1:c.1300T>A	XP_011531362.1:p.Ser434Thr
XM_011533061.1:c.1300T>A	XP_011531363.1:p.Ser434Thr
XM_011533062.1:c.1186T>A	XP_011531364.1:p.Ser396Thr
XM_011533063.1:c.1183T>A	XP_011531365.1:p.Ser395Thr
XM_011533064.1:c.1036T>A	XP_011531366.1:p.Ser346Thr
XM_011533065.1:c.1300T>A	XP_011531367.1:p.Ser434Thr
XM_011533066.1:c.142T>A	XP_011531368.1:p.Ser48Thr
XM_005264515.4:c.1207T>A	XP_005264572.1:p.Ser403Thr
XM_011533062.2:c.1186T>A	XP_011531364.1:p.Ser396Thr
XM_011533064.2:c.1036T>A	XP_011531366.1:p.Ser346Thr
NM_001382394.1:c.1186T>A	NP_001369323.1:p.Ser396Thr
NM_001382395.1:c.1207T>A	NP_001369324.1:p.Ser403Thr
NM_005633.4:c.1207T>A MANE Select	NP_005624.2:p.Ser403Thr