Canonical Allele Identifier: CA1246139725

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39022893T= , CM000664.2:g.39022893T=	GRCh38
NC_000002.11:g.39250034T= , CM000664.1:g.39250034T=	GRCh37
NC_000002.10:g.39103538T=	NCBI36
NG_007530.1:g.102571A= , LRG_754:g.102571A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000472480.2:n.1415A=
ENST00000685279.1:c.302A=	ENSP00000509424.1:p.His101=
ENST00000688043.1:n.1756A=
ENST00000689668.1:n.1542A=
ENST00000690876.1:c.1424A=	ENSP00000508955.1:p.His475=
ENST00000691229.1:c.1424A=	ENSP00000510437.1:p.His475=
ENST00000692089.1:c.1424A=	ENSP00000508626.1:p.His475=
ENST00000692620.1:c.302A=	ENSP00000509311.1:p.His101=
ENST00000402219.8:c.1535A= MANE Select	ENSP00000384675.2:p.His512=
ENST00000395038.6:c.1535A=	ENSP00000378479.2:p.His512=
ENST00000402219.6:c.1535A=	ENSP00000384675.2:p.His512=
ENST00000426016.5:c.1535A=	ENSP00000387784.1:p.His512=
ENST00000472480.1:n.379A=
NM_005633.3:c.1535A= , LRG_754t1:c.1535A=	NP_005624.2:p.His512=
XM_005264515.3:c.1535A=	XP_005264572.1:p.His512=
XM_011533060.1:c.1628A=	XP_011531362.1:p.His543=
XM_011533061.1:c.1628A=	XP_011531363.1:p.His543=
XM_011533062.1:c.1514A=	XP_011531364.1:p.His505=
XM_011533063.1:c.1511A=	XP_011531365.1:p.His504=
XM_011533064.1:c.1364A=	XP_011531366.1:p.His455=
XM_011533065.1:c.1628A=	XP_011531367.1:p.His543=
XM_011533066.1:c.470A=	XP_011531368.1:p.His157=
XM_005264515.4:c.1535A=	XP_005264572.1:p.His512=
XM_011533062.2:c.1514A=	XP_011531364.1:p.His505=
XM_011533064.2:c.1364A=	XP_011531366.1:p.His455=
NM_001382394.1:c.1514A=	NP_001369323.1:p.His505=
NM_001382395.1:c.1535A=	NP_001369324.1:p.His512=
NM_005633.4:c.1535A= MANE Select	NP_005624.2:p.His512=