Canonical Allele Identifier: CA1246139776

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39022922A= , CM000664.2:g.39022922A=	GRCh38
NC_000002.11:g.39250063A= , CM000664.1:g.39250063A=	GRCh37
NC_000002.10:g.39103567A=	NCBI36
NG_007530.1:g.102542T= , LRG_754:g.102542T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000472480.2:n.1386T=
ENST00000685279.1:c.273T=	ENSP00000509424.1:p.Asn91=
ENST00000688043.1:n.1727T=
ENST00000689668.1:n.1513T=
ENST00000690876.1:c.1395T=	ENSP00000508955.1:p.Asn465=
ENST00000691229.1:c.1395T=	ENSP00000510437.1:p.Asn465=
ENST00000692089.1:c.1395T=	ENSP00000508626.1:p.Asn465=
ENST00000692620.1:c.273T=	ENSP00000509311.1:p.Asn91=
ENST00000402219.8:c.1506T= MANE Select	ENSP00000384675.2:p.Asn502=
ENST00000395038.6:c.1506T=	ENSP00000378479.2:p.Asn502=
ENST00000402219.6:c.1506T=	ENSP00000384675.2:p.Asn502=
ENST00000426016.5:c.1506T=	ENSP00000387784.1:p.Asn502=
ENST00000472480.1:n.350T=
NM_005633.3:c.1506T= , LRG_754t1:c.1506T=	NP_005624.2:p.Asn502=
XM_005264515.3:c.1506T=	XP_005264572.1:p.Asn502=
XM_011533060.1:c.1599T=	XP_011531362.1:p.Asn533=
XM_011533061.1:c.1599T=	XP_011531363.1:p.Asn533=
XM_011533062.1:c.1485T=	XP_011531364.1:p.Asn495=
XM_011533063.1:c.1482T=	XP_011531365.1:p.Asn494=
XM_011533064.1:c.1335T=	XP_011531366.1:p.Asn445=
XM_011533065.1:c.1599T=	XP_011531367.1:p.Asn533=
XM_011533066.1:c.441T=	XP_011531368.1:p.Asn147=
XM_005264515.4:c.1506T=	XP_005264572.1:p.Asn502=
XM_011533062.2:c.1485T=	XP_011531364.1:p.Asn495=
XM_011533064.2:c.1335T=	XP_011531366.1:p.Asn445=
NM_001382394.1:c.1485T=	NP_001369323.1:p.Asn495=
NM_001382395.1:c.1506T=	NP_001369324.1:p.Asn502=
NM_005633.4:c.1506T= MANE Select	NP_005624.2:p.Asn502=