Canonical Allele Identifier: CA1246131862

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39013456A= , CM000664.2:g.39013456A=	GRCh38
NC_000002.11:g.39240597A= , CM000664.1:g.39240597A=	GRCh37
NC_000002.10:g.39094101A=	NCBI36
NG_007530.1:g.112008T= , LRG_754:g.112008T=

Transcript Alleles

HGVS	Amino-acid Change
NM_005633.4:c.2167+4T= MANE Select	NP_005624.2:n.2167+4T=
ENST00000402219.8:c.2167+4T= MANE Select	ENSP00000384675.2:n.2167+4T=
NM_001382394.1:c.2146+4T=	NP_001369323.1:n.2146+4T=
NM_001382395.1:c.2167+4T=	NP_001369324.1:n.2167+4T=
NM_005633.3:c.2167+4T= , LRG_754t1:c.2167+4T=	NP_005624.2:n.2167+4T=
ENST00000395038.6:c.2167+4T=	ENSP00000378479.2:n.2167+4T=
ENST00000402219.6:c.2167+4T=	ENSP00000384675.2:n.2167+4T=
ENST00000426016.5:c.2167+4T=	ENSP00000387784.1:n.2167+4T=
ENST00000685279.1:c.934+4T=	ENSP00000509424.1:n.934+4T=
ENST00000688043.1:n.2392T=
ENST00000689668.1:n.2174+4T=
ENST00000690514.1:n.256+4T=
ENST00000690876.1:c.2056+4T=	ENSP00000508955.1:n.2056+4T=
ENST00000691229.1:c.2056+4T=	ENSP00000510437.1:n.2056+4T=
ENST00000692089.1:c.2056+4T=	ENSP00000508626.1:n.2056+4T=
ENST00000692620.1:c.934+4T=	ENSP00000509311.1:n.934+4T=
XM_005264515.3:c.2167+4T=	XP_005264572.1:n.2167+4T=
XM_005264515.4:c.2167+4T=	XP_005264572.1:n.2167+4T=
XM_011533060.1:c.2260+4T=	XP_011531362.1:n.2260+4T=
XM_011533061.1:c.2260+4T=	XP_011531363.1:n.2260+4T=
XM_011533062.1:c.2146+4T=	XP_011531364.1:n.2146+4T=
XM_011533062.2:c.2146+4T=	XP_011531364.1:n.2146+4T=
XM_011533063.1:c.2143+4T=	XP_011531365.1:n.2143+4T=
XM_011533064.1:c.1996+4T=	XP_011531366.1:n.1996+4T=
XM_011533064.2:c.1996+4T=	XP_011531366.1:n.1996+4T=
XM_011533065.1:c.2260+4T=	XP_011531367.1:n.2260+4T=
XM_011533066.1:c.1102+4T=	XP_011531368.1:n.1102+4T=