Canonical Allele Identifier: CA425778401

Gene: SOS1

Linked Data

• MyVariant Identifiers: chr2:g.39281788G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39054647G>C , CM000664.2:g.39054647G>C	GRCh38
NC_000002.11:g.39281788G>C , CM000664.1:g.39281788G>C	GRCh37
NC_000002.10:g.39135292G>C	NCBI36
NG_007530.1:g.70817C>G , LRG_754:g.70817C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461545.2:n.714C>G
ENST00000685782.1:n.1525C>G
ENST00000688189.1:n.452C>G
ENST00000689668.1:n.694C>G
ENST00000690679.1:c.787C>G
ENST00000690876.1:c.687C>G	ENSP00000508955.1:p.Pro229=
ENST00000691229.1:c.687C>G	ENSP00000510437.1:p.Pro229=
ENST00000692089.1:c.687C>G	ENSP00000508626.1:p.Pro229=
ENST00000402219.8:c.687C>G MANE Select	ENSP00000384675.2:p.Pro229=
ENST00000395038.6:c.687C>G	ENSP00000378479.2:p.Pro229=
ENST00000402219.6:c.687C>G	ENSP00000384675.2:p.Pro229=
ENST00000426016.5:c.687C>G	ENSP00000387784.1:p.Pro229=
NM_005633.3:c.687C>G , LRG_754t1:c.687C>G	NP_005624.2:p.Pro229=
XM_005264515.3:c.687C>G	XP_005264572.1:p.Pro229=
XM_011533060.1:c.780C>G	XP_011531362.1:p.Pro260=
XM_011533061.1:c.780C>G	XP_011531363.1:p.Pro260=
XM_011533062.1:c.666C>G	XP_011531364.1:p.Pro222=
XM_011533063.1:c.663C>G	XP_011531365.1:p.Pro221=
XM_011533064.1:c.516C>G	XP_011531366.1:p.Pro172=
XM_011533065.1:c.780C>G	XP_011531367.1:p.Pro260=
XM_005264515.4:c.687C>G	XP_005264572.1:p.Pro229=
XM_011533062.2:c.666C>G	XP_011531364.1:p.Pro222=
XM_011533064.2:c.516C>G	XP_011531366.1:p.Pro172=
NM_001382394.1:c.666C>G	NP_001369323.1:p.Pro222=
NM_001382395.1:c.687C>G	NP_001369324.1:p.Pro229=
NM_005633.4:c.687C>G MANE Select	NP_005624.2:p.Pro229=