Canonical Allele Identifier: CA1246139093

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39022539_39022541delinsCAA , CM000664.2:g.39022539_39022541delinsCAA	GRCh38
NC_000002.11:g.39249680_39249682delinsCAA , CM000664.1:g.39249680_39249682delinsCAA	GRCh37
NC_000002.10:g.39103184_39103186delinsCAA	NCBI36
NG_007530.1:g.102923_102925delinsTTG , LRG_754:g.102923_102925delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000472480.2:n.1767_1769delinsTTG
ENST00000685279.1:c.625+29_625+31delinsTTG	ENSP00000509424.1:n.625+29_625+31delinsTTG
ENST00000688043.1:n.2079+29_2079+31delinsTTG
ENST00000689668.1:n.1865+29_1865+31delinsTTG
ENST00000690876.1:c.1747+29_1747+31delinsTTG	ENSP00000508955.1:n.1747+29_1747+31delinsTTG
ENST00000691229.1:c.1747+29_1747+31delinsTTG	ENSP00000510437.1:n.1747+29_1747+31delinsTTG
ENST00000692089.1:c.1747+29_1747+31delinsTTG	ENSP00000508626.1:n.1747+29_1747+31delinsTTG
ENST00000692620.1:c.625+29_625+31delinsTTG	ENSP00000509311.1:n.625+29_625+31delinsTTG
ENST00000402219.8:c.1858+29_1858+31delinsTTG MANE Select	ENSP00000384675.2:n.1858+29_1858+31delinsTTG
ENST00000395038.6:c.1858+29_1858+31delinsTTG	ENSP00000378479.2:n.1858+29_1858+31delinsTTG
ENST00000402219.6:c.1858+29_1858+31delinsTTG	ENSP00000384675.2:n.1858+29_1858+31delinsTTG
ENST00000426016.5:c.1858+29_1858+31delinsTTG	ENSP00000387784.1:n.1858+29_1858+31delinsTTG
NM_005633.3:c.1858+29_1858+31delinsTTG , LRG_754t1:c.1858+29_1858+31delinsTTG	NP_005624.2:n.1858+29_1858+31delinsTTG
XM_005264515.3:c.1858+29_1858+31delinsTTG	XP_005264572.1:n.1858+29_1858+31delinsTTG
XM_011533060.1:c.1951+29_1951+31delinsTTG	XP_011531362.1:n.1951+29_1951+31delinsTTG
XM_011533061.1:c.1951+29_1951+31delinsTTG	XP_011531363.1:n.1951+29_1951+31delinsTTG
XM_011533062.1:c.1837+29_1837+31delinsTTG	XP_011531364.1:n.1837+29_1837+31delinsTTG
XM_011533063.1:c.1834+29_1834+31delinsTTG	XP_011531365.1:n.1834+29_1834+31delinsTTG
XM_011533064.1:c.1687+29_1687+31delinsTTG	XP_011531366.1:n.1687+29_1687+31delinsTTG
XM_011533065.1:c.1951+29_1951+31delinsTTG	XP_011531367.1:n.1951+29_1951+31delinsTTG
XM_011533066.1:c.793+29_793+31delinsTTG	XP_011531368.1:n.793+29_793+31delinsTTG
XM_005264515.4:c.1858+29_1858+31delinsTTG	XP_005264572.1:n.1858+29_1858+31delinsTTG
XM_011533062.2:c.1837+29_1837+31delinsTTG	XP_011531364.1:n.1837+29_1837+31delinsTTG
XM_011533064.2:c.1687+29_1687+31delinsTTG	XP_011531366.1:n.1687+29_1687+31delinsTTG
NM_001382394.1:c.1837+29_1837+31delinsTTG	NP_001369323.1:n.1837+29_1837+31delinsTTG
NM_001382395.1:c.1858+29_1858+31delinsTTG	NP_001369324.1:n.1858+29_1858+31delinsTTG
NM_005633.4:c.1858+29_1858+31delinsTTG MANE Select	NP_005624.2:n.1858+29_1858+31delinsTTG