Canonical Allele Identifier: CA2749574487

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39022470_39022472del , CM000664.2:g.39022470_39022472del	GRCh38
NC_000002.11:g.39249611_39249613del , CM000664.1:g.39249611_39249613del	GRCh37
NC_000002.10:g.39103115_39103117del	NCBI36
NG_007530.1:g.102995_102997del , LRG_754:g.102995_102997del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000472480.2:n.1839_1841del
ENST00000685279.1:c.625+101_625+103del	ENSP00000509424.1:n.625+101_625+103del
ENST00000688043.1:n.2079+101_2079+103del
ENST00000689668.1:n.1865+101_1865+103del
ENST00000690876.1:c.1747+101_1747+103del	ENSP00000508955.1:n.1747+101_1747+103del
ENST00000691229.1:c.1747+101_1747+103del	ENSP00000510437.1:n.1747+101_1747+103del
ENST00000692089.1:c.1747+101_1747+103del	ENSP00000508626.1:n.1747+101_1747+103del
ENST00000692620.1:c.625+101_625+103del	ENSP00000509311.1:n.625+101_625+103del
ENST00000402219.8:c.1858+101_1858+103del MANE Select	ENSP00000384675.2:n.1858+101_1858+103del
ENST00000395038.6:c.1858+101_1858+103del	ENSP00000378479.2:n.1858+101_1858+103del
ENST00000402219.6:c.1858+101_1858+103del	ENSP00000384675.2:n.1858+101_1858+103del
ENST00000426016.5:c.1858+101_1858+103del	ENSP00000387784.1:n.1858+101_1858+103del
NM_005633.3:c.1858+101_1858+103del , LRG_754t1:c.1858+101_1858+103del	NP_005624.2:n.1858+101_1858+103del
XM_005264515.3:c.1858+101_1858+103del	XP_005264572.1:n.1858+101_1858+103del
XM_011533060.1:c.1951+101_1951+103del	XP_011531362.1:n.1951+101_1951+103del
XM_011533061.1:c.1951+101_1951+103del	XP_011531363.1:n.1951+101_1951+103del
XM_011533062.1:c.1837+101_1837+103del	XP_011531364.1:n.1837+101_1837+103del
XM_011533063.1:c.1834+101_1834+103del	XP_011531365.1:n.1834+101_1834+103del
XM_011533064.1:c.1687+101_1687+103del	XP_011531366.1:n.1687+101_1687+103del
XM_011533065.1:c.1951+101_1951+103del	XP_011531367.1:n.1951+101_1951+103del
XM_011533066.1:c.793+101_793+103del	XP_011531368.1:n.793+101_793+103del
XM_005264515.4:c.1858+101_1858+103del	XP_005264572.1:n.1858+101_1858+103del
XM_011533062.2:c.1837+101_1837+103del	XP_011531364.1:n.1837+101_1837+103del
XM_011533064.2:c.1687+101_1687+103del	XP_011531366.1:n.1687+101_1687+103del
NM_001382394.1:c.1837+101_1837+103del	NP_001369323.1:n.1837+101_1837+103del
NM_001382395.1:c.1858+101_1858+103del	NP_001369324.1:n.1858+101_1858+103del
NM_005633.4:c.1858+101_1858+103del MANE Select	NP_005624.2:n.1858+101_1858+103del