Canonical Allele Identifier: CA1246123964

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38997072T= , CM000664.2:g.38997072T=	GRCh38
NC_000002.11:g.39224213T= , CM000664.1:g.39224213T=	GRCh37
NC_000002.10:g.39077717T=	NCBI36
NG_007530.1:g.128392A= , LRG_754:g.128392A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685279.1:c.1732-34A=	ENSP00000509424.1:n.1732-34A=
ENST00000689668.1:n.2972-34A=
ENST00000690876.1:c.*271-34A=	ENSP00000508955.1:n.*271-34A=
ENST00000691229.1:c.2734-34A=	ENSP00000510437.1:n.2734-34A=
ENST00000692089.1:c.2854-34A=	ENSP00000508626.1:n.2854-34A=
ENST00000692227.1:c.661-34A=	ENSP00000509138.1:n.661-34A=
ENST00000692620.1:c.*552-34A=	ENSP00000509311.1:n.*552-34A=
ENST00000402219.8:c.2965-34A= MANE Select	ENSP00000384675.2:n.2965-34A=
ENST00000395038.6:c.2965-34A=	ENSP00000378479.2:n.2965-34A=
ENST00000402219.6:c.2965-34A=	ENSP00000384675.2:n.2965-34A=
ENST00000426016.5:c.2965-34A=	ENSP00000387784.1:n.2965-34A=
NM_005633.3:c.2965-34A= , LRG_754t1:c.2965-34A=	NP_005624.2:n.2965-34A=
XM_005264515.3:c.2965-34A=	XP_005264572.1:n.2965-34A=
XM_011533060.1:c.3058-34A=	XP_011531362.1:n.3058-34A=
XM_011533061.1:c.3058-34A=	XP_011531363.1:n.3058-34A=
XM_011533062.1:c.2944-34A=	XP_011531364.1:n.2944-34A=
XM_011533063.1:c.2941-34A=	XP_011531365.1:n.2941-34A=
XM_011533064.1:c.2794-34A=	XP_011531366.1:n.2794-34A=
XM_011533065.1:c.3058-34A=	XP_011531367.1:n.3058-34A=
XM_011533066.1:c.1900-34A=	XP_011531368.1:n.1900-34A=
XM_005264515.4:c.2965-34A=	XP_005264572.1:n.2965-34A=
XM_011533062.2:c.2944-34A=	XP_011531364.1:n.2944-34A=
XM_011533064.2:c.2794-34A=	XP_011531366.1:n.2794-34A=
NM_001382394.1:c.2944-34A=	NP_001369323.1:n.2944-34A=
NM_001382395.1:c.2965-34A=	NP_001369324.1:n.2965-34A=
NM_005633.4:c.2965-34A= MANE Select	NP_005624.2:n.2965-34A=