Canonical Allele Identifier: CA346367393

Gene: SOS1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39035440C>T , CM000664.2:g.39035440C>T	GRCh38
NC_000002.11:g.39262581C>T , CM000664.1:g.39262581C>T	GRCh37
NC_000002.10:g.39116085C>T	NCBI36
NG_007530.1:g.90024G>A , LRG_754:g.90024G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461545.2:n.952G>A
ENST00000472480.2:n.805G>A
ENST00000685782.1:n.1763G>A
ENST00000689668.1:n.932G>A
ENST00000690679.1:c.1025G>A
ENST00000690876.1:c.865-130G>A	ENSP00000508955.1:n.865-130G>A
ENST00000691229.1:c.865-130G>A	ENSP00000510437.1:n.865-130G>A
ENST00000692089.1:c.865-130G>A	ENSP00000508626.1:n.865-130G>A
ENST00000402219.8:c.925G>A MANE Select	ENSP00000384675.2:p.Asp309Asn
ENST00000395038.6:c.925G>A	ENSP00000378479.2:p.Asp309Asn
ENST00000402219.6:c.925G>A	ENSP00000384675.2:p.Asp309Asn
ENST00000426016.5:c.925G>A	ENSP00000387784.1:p.Asp309Asn
ENST00000461545.1:n.275G>A
NM_005633.3:c.925G>A , LRG_754t1:c.925G>A	NP_005624.2:p.Asp309Asn
XM_005264515.3:c.925G>A	XP_005264572.1:p.Asp309Asn
XM_011533060.1:c.1018G>A	XP_011531362.1:p.Asp340Asn
XM_011533061.1:c.1018G>A	XP_011531363.1:p.Asp340Asn
XM_011533062.1:c.904G>A	XP_011531364.1:p.Asp302Asn
XM_011533063.1:c.901G>A	XP_011531365.1:p.Asp301Asn
XM_011533064.1:c.754G>A	XP_011531366.1:p.Asp252Asn
XM_011533065.1:c.1018G>A	XP_011531367.1:p.Asp340Asn
XM_005264515.4:c.925G>A	XP_005264572.1:p.Asp309Asn
XM_011533062.2:c.904G>A	XP_011531364.1:p.Asp302Asn
XM_011533064.2:c.754G>A	XP_011531366.1:p.Asp252Asn
NM_001382394.1:c.904G>A	NP_001369323.1:p.Asp302Asn
NM_001382395.1:c.925G>A	NP_001369324.1:p.Asp309Asn
NM_005633.4:c.925G>A MANE Select	NP_005624.2:p.Asp309Asn