Canonical Allele Identifier: CA1246150378

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39051211G= , CM000664.2:g.39051211G=	GRCh38
NC_000002.11:g.39278352G= , CM000664.1:g.39278352G=	GRCh37
NC_000002.10:g.39131856G=	NCBI36
NG_007530.1:g.74253C= , LRG_754:g.74253C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461545.2:n.824C=
ENST00000472480.2:n.677C=
ENST00000685782.1:n.1635C=
ENST00000689668.1:n.804C=
ENST00000690679.1:c.897C=
ENST00000690876.1:c.797C=	ENSP00000508955.1:p.Thr266=
ENST00000691229.1:c.797C=	ENSP00000510437.1:p.Thr266=
ENST00000692089.1:c.797C=	ENSP00000508626.1:p.Thr266=
ENST00000402219.8:c.797C= MANE Select	ENSP00000384675.2:p.Thr266=
ENST00000395038.6:c.797C=	ENSP00000378479.2:p.Thr266=
ENST00000402219.6:c.797C=	ENSP00000384675.2:p.Thr266=
ENST00000426016.5:c.797C=	ENSP00000387784.1:p.Thr266=
ENST00000461545.1:n.147C=
NM_005633.3:c.797C= , LRG_754t1:c.797C=	NP_005624.2:p.Thr266=
XM_005264515.3:c.797C=	XP_005264572.1:p.Thr266=
XM_011533060.1:c.890C=	XP_011531362.1:p.Thr297=
XM_011533061.1:c.890C=	XP_011531363.1:p.Thr297=
XM_011533062.1:c.776C=	XP_011531364.1:p.Thr259=
XM_011533063.1:c.773C=	XP_011531365.1:p.Thr258=
XM_011533064.1:c.626C=	XP_011531366.1:p.Thr209=
XM_011533065.1:c.890C=	XP_011531367.1:p.Thr297=
XM_005264515.4:c.797C=	XP_005264572.1:p.Thr266=
XM_011533062.2:c.776C=	XP_011531364.1:p.Thr259=
XM_011533064.2:c.626C=	XP_011531366.1:p.Thr209=
NM_001382394.1:c.776C=	NP_001369323.1:p.Thr259=
NM_001382395.1:c.797C=	NP_001369324.1:p.Thr266=
NM_005633.4:c.797C= MANE Select	NP_005624.2:p.Thr266=