Canonical Allele Identifier: CA1246139487

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39022777_39022780delinsCCAG , CM000664.2:g.39022777_39022780delinsCCAG	GRCh38
NC_000002.11:g.39249918_39249921delinsCCAG , CM000664.1:g.39249918_39249921delinsCCAG	GRCh37
NC_000002.10:g.39103422_39103425delinsCCAG	NCBI36
NG_007530.1:g.102684_102687delinsCTGG , LRG_754:g.102684_102687delinsCTGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000472480.2:n.1528_1531delinsCTGG
ENST00000685279.1:c.415_418delinsCTGG	ENSP00000509424.1:p.Leu139=
ENST00000688043.1:n.1869_1872delinsCTGG
ENST00000689668.1:n.1655_1658delinsCTGG
ENST00000690876.1:c.1537_1540delinsCTGG	ENSP00000508955.1:p.Leu513=
ENST00000691229.1:c.1537_1540delinsCTGG	ENSP00000510437.1:p.Leu513=
ENST00000692089.1:c.1537_1540delinsCTGG	ENSP00000508626.1:p.Leu513=
ENST00000692620.1:c.415_418delinsCTGG	ENSP00000509311.1:p.Leu139=
ENST00000402219.8:c.1648_1651delinsCTGG MANE Select	ENSP00000384675.2:p.Leu550=
ENST00000395038.6:c.1648_1651delinsCTGG	ENSP00000378479.2:p.Leu550=
ENST00000402219.6:c.1648_1651delinsCTGG	ENSP00000384675.2:p.Leu550=
ENST00000426016.5:c.1648_1651delinsCTGG	ENSP00000387784.1:p.Leu550=
NM_005633.3:c.1648_1651delinsCTGG , LRG_754t1:c.1648_1651delinsCTGG	NP_005624.2:p.Leu550=
XM_005264515.3:c.1648_1651delinsCTGG	XP_005264572.1:p.Leu550=
XM_011533060.1:c.1741_1744delinsCTGG	XP_011531362.1:p.Leu581=
XM_011533061.1:c.1741_1744delinsCTGG	XP_011531363.1:p.Leu581=
XM_011533062.1:c.1627_1630delinsCTGG	XP_011531364.1:p.Leu543=
XM_011533063.1:c.1624_1627delinsCTGG	XP_011531365.1:p.Leu542=
XM_011533064.1:c.1477_1480delinsCTGG	XP_011531366.1:p.Leu493=
XM_011533065.1:c.1741_1744delinsCTGG	XP_011531367.1:p.Leu581=
XM_011533066.1:c.583_586delinsCTGG	XP_011531368.1:p.Leu195=
XM_005264515.4:c.1648_1651delinsCTGG	XP_005264572.1:p.Leu550=
XM_011533062.2:c.1627_1630delinsCTGG	XP_011531364.1:p.Leu543=
XM_011533064.2:c.1477_1480delinsCTGG	XP_011531366.1:p.Leu493=
NM_001382394.1:c.1627_1630delinsCTGG	NP_001369323.1:p.Leu543=
NM_001382395.1:c.1648_1651delinsCTGG	NP_001369324.1:p.Leu550=
NM_005633.4:c.1648_1651delinsCTGG MANE Select	NP_005624.2:p.Leu550=