Canonical Allele Identifier: CA2562239013

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39022525_39022526insA , CM000664.2:g.39022525_39022526insA	GRCh38
NC_000002.11:g.39249666_39249667insA , CM000664.1:g.39249666_39249667insA	GRCh37
NC_000002.10:g.39103170_39103171insA	NCBI36
NG_007530.1:g.102938_102939insT , LRG_754:g.102938_102939insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000472480.2:n.1782_1783insT
ENST00000685279.1:c.625+44_625+45insT	ENSP00000509424.1:n.625+44_625+45insT
ENST00000688043.1:n.2079+44_2079+45insT
ENST00000689668.1:n.1865+44_1865+45insT
ENST00000690876.1:c.1747+44_1747+45insT	ENSP00000508955.1:n.1747+44_1747+45insT
ENST00000691229.1:c.1747+44_1747+45insT	ENSP00000510437.1:n.1747+44_1747+45insT
ENST00000692089.1:c.1747+44_1747+45insT	ENSP00000508626.1:n.1747+44_1747+45insT
ENST00000692620.1:c.625+44_625+45insT	ENSP00000509311.1:n.625+44_625+45insT
ENST00000402219.8:c.1858+44_1858+45insT MANE Select	ENSP00000384675.2:n.1858+44_1858+45insT
ENST00000395038.6:c.1858+44_1858+45insT	ENSP00000378479.2:n.1858+44_1858+45insT
ENST00000402219.6:c.1858+44_1858+45insT	ENSP00000384675.2:n.1858+44_1858+45insT
ENST00000426016.5:c.1858+44_1858+45insT	ENSP00000387784.1:n.1858+44_1858+45insT
NM_005633.3:c.1858+44_1858+45insT , LRG_754t1:c.1858+44_1858+45insT	NP_005624.2:n.1858+44_1858+45insT
XM_005264515.3:c.1858+44_1858+45insT	XP_005264572.1:n.1858+44_1858+45insT
XM_011533060.1:c.1951+44_1951+45insT	XP_011531362.1:n.1951+44_1951+45insT
XM_011533061.1:c.1951+44_1951+45insT	XP_011531363.1:n.1951+44_1951+45insT
XM_011533062.1:c.1837+44_1837+45insT	XP_011531364.1:n.1837+44_1837+45insT
XM_011533063.1:c.1834+44_1834+45insT	XP_011531365.1:n.1834+44_1834+45insT
XM_011533064.1:c.1687+44_1687+45insT	XP_011531366.1:n.1687+44_1687+45insT
XM_011533065.1:c.1951+44_1951+45insT	XP_011531367.1:n.1951+44_1951+45insT
XM_011533066.1:c.793+44_793+45insT	XP_011531368.1:n.793+44_793+45insT
XM_005264515.4:c.1858+44_1858+45insT	XP_005264572.1:n.1858+44_1858+45insT
XM_011533062.2:c.1837+44_1837+45insT	XP_011531364.1:n.1837+44_1837+45insT
XM_011533064.2:c.1687+44_1687+45insT	XP_011531366.1:n.1687+44_1687+45insT
NM_001382394.1:c.1837+44_1837+45insT	NP_001369323.1:n.1837+44_1837+45insT
NM_001382395.1:c.1858+44_1858+45insT	NP_001369324.1:n.1858+44_1858+45insT
NM_005633.4:c.1858+44_1858+45insT MANE Select	NP_005624.2:n.1858+44_1858+45insT