Canonical Allele Identifier: CA1624610

Gene: SOS1

Linked Data

• ClinVar Variation Id: 381373
• ClinVar RCV Id: RCV000421562 ; RCV002062419 ; RCV002467782 ; RCV002467783 ; RCV004022340
• dbSNP Id: rs138459502
• ExAC: 2:39250300 G / A
• gnomAD v2: 2-39250300-G-A
• gnomAD v3: 2-39023159-G-A
• gnomAD v4: 2-39023159-G-A
• MyVariant Identifiers: chr2:g.39250300G>A (hg19) ; chr2:g.39023159G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39023159G>A , CM000664.2:g.39023159G>A	GRCh38
NC_000002.11:g.39250300G>A , CM000664.1:g.39250300G>A	GRCh37
NC_000002.10:g.39103804G>A	NCBI36
NG_007530.1:g.102305C>T , LRG_754:g.102305C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000472480.2:n.1149C>T
ENST00000685279.1:c.36C>T	ENSP00000509424.1:p.Asn12=
ENST00000688043.1:n.1490C>T
ENST00000689668.1:n.1276C>T
ENST00000690679.1:c.1456C>T
ENST00000690876.1:c.1158C>T	ENSP00000508955.1:p.Asn386=
ENST00000691229.1:c.1158C>T	ENSP00000510437.1:p.Asn386=
ENST00000692089.1:c.1158C>T	ENSP00000508626.1:p.Asn386=
ENST00000692620.1:c.36C>T	ENSP00000509311.1:p.Asn12=
ENST00000402219.8:c.1269C>T MANE Select	ENSP00000384675.2:p.Asn423=
ENST00000395038.6:c.1269C>T	ENSP00000378479.2:p.Asn423=
ENST00000402219.6:c.1269C>T	ENSP00000384675.2:p.Asn423=
ENST00000426016.5:c.1269C>T	ENSP00000387784.1:p.Asn423=
ENST00000472480.1:n.113C>T
NM_005633.3:c.1269C>T , LRG_754t1:c.1269C>T	NP_005624.2:p.Asn423=
XM_005264515.3:c.1269C>T	XP_005264572.1:p.Asn423=
XM_011533060.1:c.1362C>T	XP_011531362.1:p.Asn454=
XM_011533061.1:c.1362C>T	XP_011531363.1:p.Asn454=
XM_011533062.1:c.1248C>T	XP_011531364.1:p.Asn416=
XM_011533063.1:c.1245C>T	XP_011531365.1:p.Asn415=
XM_011533064.1:c.1098C>T	XP_011531366.1:p.Asn366=
XM_011533065.1:c.1362C>T	XP_011531367.1:p.Asn454=
XM_011533066.1:c.204C>T	XP_011531368.1:p.Asn68=
XM_005264515.4:c.1269C>T	XP_005264572.1:p.Asn423=
XM_011533062.2:c.1248C>T	XP_011531364.1:p.Asn416=
XM_011533064.2:c.1098C>T	XP_011531366.1:p.Asn366=
NM_001382394.1:c.1248C>T	NP_001369323.1:p.Asn416=
NM_001382395.1:c.1269C>T	NP_001369324.1:p.Asn423=
NM_005633.4:c.1269C>T MANE Select	NP_005624.2:p.Asn423=