Canonical Allele Identifier: CA346366031

Gene: SOS1

Linked Data

• MyVariant Identifiers: chr2:g.39250068T>C (hg19) ; chr2:g.39022927T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39022927T>C , CM000664.2:g.39022927T>C	GRCh38
NC_000002.11:g.39250068T>C , CM000664.1:g.39250068T>C	GRCh37
NC_000002.10:g.39103572T>C	NCBI36
NG_007530.1:g.102537A>G , LRG_754:g.102537A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000472480.2:n.1381A>G
ENST00000685279.1:c.268A>G	ENSP00000509424.1:p.Ile90Val
ENST00000688043.1:n.1722A>G
ENST00000689668.1:n.1508A>G
ENST00000690876.1:c.1390A>G	ENSP00000508955.1:p.Ile464Val
ENST00000691229.1:c.1390A>G	ENSP00000510437.1:p.Ile464Val
ENST00000692089.1:c.1390A>G	ENSP00000508626.1:p.Ile464Val
ENST00000692620.1:c.268A>G	ENSP00000509311.1:p.Ile90Val
ENST00000402219.8:c.1501A>G MANE Select	ENSP00000384675.2:p.Ile501Val
ENST00000395038.6:c.1501A>G	ENSP00000378479.2:p.Ile501Val
ENST00000402219.6:c.1501A>G	ENSP00000384675.2:p.Ile501Val
ENST00000426016.5:c.1501A>G	ENSP00000387784.1:p.Ile501Val
ENST00000472480.1:n.345A>G
NM_005633.3:c.1501A>G , LRG_754t1:c.1501A>G	NP_005624.2:p.Ile501Val
XM_005264515.3:c.1501A>G	XP_005264572.1:p.Ile501Val
XM_011533060.1:c.1594A>G	XP_011531362.1:p.Ile532Val
XM_011533061.1:c.1594A>G	XP_011531363.1:p.Ile532Val
XM_011533062.1:c.1480A>G	XP_011531364.1:p.Ile494Val
XM_011533063.1:c.1477A>G	XP_011531365.1:p.Ile493Val
XM_011533064.1:c.1330A>G	XP_011531366.1:p.Ile444Val
XM_011533065.1:c.1594A>G	XP_011531367.1:p.Ile532Val
XM_011533066.1:c.436A>G	XP_011531368.1:p.Ile146Val
XM_005264515.4:c.1501A>G	XP_005264572.1:p.Ile501Val
XM_011533062.2:c.1480A>G	XP_011531364.1:p.Ile494Val
XM_011533064.2:c.1330A>G	XP_011531366.1:p.Ile444Val
NM_001382394.1:c.1480A>G	NP_001369323.1:p.Ile494Val
NM_001382395.1:c.1501A>G	NP_001369324.1:p.Ile501Val
NM_005633.4:c.1501A>G MANE Select	NP_005624.2:p.Ile501Val