Canonical Allele Identifier: CA346366385

Gene: SOS1

Linked Data

• MyVariant Identifiers: chr2:g.39250227C>T (hg19) ; chr2:g.39023086C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39023086C>T , CM000664.2:g.39023086C>T	GRCh38
NC_000002.11:g.39250227C>T , CM000664.1:g.39250227C>T	GRCh37
NC_000002.10:g.39103731C>T	NCBI36
NG_007530.1:g.102378G>A , LRG_754:g.102378G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000472480.2:n.1222G>A
ENST00000685279.1:c.109G>A	ENSP00000509424.1:p.Gly37Arg
ENST00000688043.1:n.1563G>A
ENST00000689668.1:n.1349G>A
ENST00000690876.1:c.1231G>A	ENSP00000508955.1:p.Gly411Arg
ENST00000691229.1:c.1231G>A	ENSP00000510437.1:p.Gly411Arg
ENST00000692089.1:c.1231G>A	ENSP00000508626.1:p.Gly411Arg
ENST00000692620.1:c.109G>A	ENSP00000509311.1:p.Gly37Arg
ENST00000402219.8:c.1342G>A MANE Select	ENSP00000384675.2:p.Gly448Arg
ENST00000395038.6:c.1342G>A	ENSP00000378479.2:p.Gly448Arg
ENST00000402219.6:c.1342G>A	ENSP00000384675.2:p.Gly448Arg
ENST00000426016.5:c.1342G>A	ENSP00000387784.1:p.Gly448Arg
ENST00000472480.1:n.186G>A
NM_005633.3:c.1342G>A , LRG_754t1:c.1342G>A	NP_005624.2:p.Gly448Arg
XM_005264515.3:c.1342G>A	XP_005264572.1:p.Gly448Arg
XM_011533060.1:c.1435G>A	XP_011531362.1:p.Gly479Arg
XM_011533061.1:c.1435G>A	XP_011531363.1:p.Gly479Arg
XM_011533062.1:c.1321G>A	XP_011531364.1:p.Gly441Arg
XM_011533063.1:c.1318G>A	XP_011531365.1:p.Gly440Arg
XM_011533064.1:c.1171G>A	XP_011531366.1:p.Gly391Arg
XM_011533065.1:c.1435G>A	XP_011531367.1:p.Gly479Arg
XM_011533066.1:c.277G>A	XP_011531368.1:p.Gly93Arg
XM_005264515.4:c.1342G>A	XP_005264572.1:p.Gly448Arg
XM_011533062.2:c.1321G>A	XP_011531364.1:p.Gly441Arg
XM_011533064.2:c.1171G>A	XP_011531366.1:p.Gly391Arg
NM_001382394.1:c.1321G>A	NP_001369323.1:p.Gly441Arg
NM_001382395.1:c.1342G>A	NP_001369324.1:p.Gly448Arg
NM_005633.4:c.1342G>A MANE Select	NP_005624.2:p.Gly448Arg