Canonical Allele Identifier: CA346373001

Gene: SOS1

Linked Data

• MyVariant Identifiers: chr2:g.39281801A>C (hg19) ; chr2:g.39054660A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39054660A>C , CM000664.2:g.39054660A>C	GRCh38
NC_000002.11:g.39281801A>C , CM000664.1:g.39281801A>C	GRCh37
NC_000002.10:g.39135305A>C	NCBI36
NG_007530.1:g.70804T>G , LRG_754:g.70804T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461545.2:n.701T>G
ENST00000685782.1:n.1512T>G
ENST00000688189.1:n.439T>G
ENST00000689668.1:n.681T>G
ENST00000690679.1:c.774T>G
ENST00000690876.1:c.674T>G	ENSP00000508955.1:p.Val225Gly
ENST00000691229.1:c.674T>G	ENSP00000510437.1:p.Val225Gly
ENST00000692089.1:c.674T>G	ENSP00000508626.1:p.Val225Gly
ENST00000402219.8:c.674T>G MANE Select	ENSP00000384675.2:p.Val225Gly
ENST00000395038.6:c.674T>G	ENSP00000378479.2:p.Val225Gly
ENST00000402219.6:c.674T>G	ENSP00000384675.2:p.Val225Gly
ENST00000426016.5:c.674T>G	ENSP00000387784.1:p.Val225Gly
NM_005633.3:c.674T>G , LRG_754t1:c.674T>G	NP_005624.2:p.Val225Gly
XM_005264515.3:c.674T>G	XP_005264572.1:p.Val225Gly
XM_011533060.1:c.767T>G	XP_011531362.1:p.Val256Gly
XM_011533061.1:c.767T>G	XP_011531363.1:p.Val256Gly
XM_011533062.1:c.653T>G	XP_011531364.1:p.Val218Gly
XM_011533063.1:c.650T>G	XP_011531365.1:p.Val217Gly
XM_011533064.1:c.503T>G	XP_011531366.1:p.Val168Gly
XM_011533065.1:c.767T>G	XP_011531367.1:p.Val256Gly
XM_005264515.4:c.674T>G	XP_005264572.1:p.Val225Gly
XM_011533062.2:c.653T>G	XP_011531364.1:p.Val218Gly
XM_011533064.2:c.503T>G	XP_011531366.1:p.Val168Gly
NM_001382394.1:c.653T>G	NP_001369323.1:p.Val218Gly
NM_001382395.1:c.674T>G	NP_001369324.1:p.Val225Gly
NM_005633.4:c.674T>G MANE Select	NP_005624.2:p.Val225Gly