Canonical Allele Identifier: CA346366055

Gene: SOS1

Linked Data

• gnomAD v4: 2-39022939-G-C
• MyVariant Identifiers: chr2:g.39250080G>C (hg19) ; chr2:g.39022939G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39022939G>C , CM000664.2:g.39022939G>C	GRCh38
NC_000002.11:g.39250080G>C , CM000664.1:g.39250080G>C	GRCh37
NC_000002.10:g.39103584G>C	NCBI36
NG_007530.1:g.102525C>G , LRG_754:g.102525C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000472480.2:n.1369C>G
ENST00000685279.1:c.256C>G	ENSP00000509424.1:p.Arg86Gly
ENST00000688043.1:n.1710C>G
ENST00000689668.1:n.1496C>G
ENST00000690876.1:c.1378C>G	ENSP00000508955.1:p.Arg460Gly
ENST00000691229.1:c.1378C>G	ENSP00000510437.1:p.Arg460Gly
ENST00000692089.1:c.1378C>G	ENSP00000508626.1:p.Arg460Gly
ENST00000692620.1:c.256C>G	ENSP00000509311.1:p.Arg86Gly
ENST00000402219.8:c.1489C>G MANE Select	ENSP00000384675.2:p.Arg497Gly
ENST00000395038.6:c.1489C>G	ENSP00000378479.2:p.Arg497Gly
ENST00000402219.6:c.1489C>G	ENSP00000384675.2:p.Arg497Gly
ENST00000426016.5:c.1489C>G	ENSP00000387784.1:p.Arg497Gly
ENST00000472480.1:n.333C>G
NM_005633.3:c.1489C>G , LRG_754t1:c.1489C>G	NP_005624.2:p.Arg497Gly
XM_005264515.3:c.1489C>G	XP_005264572.1:p.Arg497Gly
XM_011533060.1:c.1582C>G	XP_011531362.1:p.Arg528Gly
XM_011533061.1:c.1582C>G	XP_011531363.1:p.Arg528Gly
XM_011533062.1:c.1468C>G	XP_011531364.1:p.Arg490Gly
XM_011533063.1:c.1465C>G	XP_011531365.1:p.Arg489Gly
XM_011533064.1:c.1318C>G	XP_011531366.1:p.Arg440Gly
XM_011533065.1:c.1582C>G	XP_011531367.1:p.Arg528Gly
XM_011533066.1:c.424C>G	XP_011531368.1:p.Arg142Gly
XM_005264515.4:c.1489C>G	XP_005264572.1:p.Arg497Gly
XM_011533062.2:c.1468C>G	XP_011531364.1:p.Arg490Gly
XM_011533064.2:c.1318C>G	XP_011531366.1:p.Arg440Gly
NM_001382394.1:c.1468C>G	NP_001369323.1:p.Arg490Gly
NM_001382395.1:c.1489C>G	NP_001369324.1:p.Arg497Gly
NM_005633.4:c.1489C>G MANE Select	NP_005624.2:p.Arg497Gly