Canonical Allele Identifier: CA1246153831

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39054671T= , CM000664.2:g.39054671T=	GRCh38
NC_000002.11:g.39281812T= , CM000664.1:g.39281812T=	GRCh37
NC_000002.10:g.39135316T=	NCBI36
NG_007530.1:g.70793A= , LRG_754:g.70793A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461545.2:n.690A=
ENST00000685782.1:n.1501A=
ENST00000688189.1:n.428A=
ENST00000689668.1:n.670A=
ENST00000690679.1:c.763A=
ENST00000690876.1:c.663A=	ENSP00000508955.1:p.Leu221=
ENST00000691229.1:c.663A=	ENSP00000510437.1:p.Leu221=
ENST00000692089.1:c.663A=	ENSP00000508626.1:p.Leu221=
ENST00000402219.8:c.663A= MANE Select	ENSP00000384675.2:p.Leu221=
ENST00000395038.6:c.663A=	ENSP00000378479.2:p.Leu221=
ENST00000402219.6:c.663A=	ENSP00000384675.2:p.Leu221=
ENST00000426016.5:c.663A=	ENSP00000387784.1:p.Leu221=
NM_005633.3:c.663A= , LRG_754t1:c.663A=	NP_005624.2:p.Leu221=
XM_005264515.3:c.663A=	XP_005264572.1:p.Leu221=
XM_011533060.1:c.756A=	XP_011531362.1:p.Leu252=
XM_011533061.1:c.756A=	XP_011531363.1:p.Leu252=
XM_011533062.1:c.642A=	XP_011531364.1:p.Leu214=
XM_011533063.1:c.639A=	XP_011531365.1:p.Leu213=
XM_011533064.1:c.492A=	XP_011531366.1:p.Leu164=
XM_011533065.1:c.756A=	XP_011531367.1:p.Leu252=
XM_005264515.4:c.663A=	XP_005264572.1:p.Leu221=
XM_011533062.2:c.642A=	XP_011531364.1:p.Leu214=
XM_011533064.2:c.492A=	XP_011531366.1:p.Leu164=
NM_001382394.1:c.642A=	NP_001369323.1:p.Leu214=
NM_001382395.1:c.663A=	NP_001369324.1:p.Leu221=
NM_005633.4:c.663A= MANE Select	NP_005624.2:p.Leu221=