Canonical Allele Identifier: CA2136084684

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180679_50180682delinsGCTC , CM000676.2:g.50180679_50180682delinsGCTC	GRCh38
NC_000014.8:g.50647397_50647400delinsGCTC , CM000676.1:g.50647397_50647400delinsGCTC	GRCh37
NC_000014.7:g.49717147_49717150delinsGCTC	NCBI36
NG_051073.1:g.56012_56015delinsGAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859_862delinsGAGC MANE Select	ENSP00000216373.5:p.Glu287=
ENST00000216373.9:c.859_862delinsGAGC	ENSP00000216373.5:p.Glu287=
ENST00000543680.5:c.859_862delinsGAGC	ENSP00000445328.1:p.Glu287=
NM_006939.2:c.859_862delinsGAGC	NP_008870.2:p.Glu287=
XM_005268021.1:c.679_682delinsGAGC	XP_005268078.1:p.Glu227=
XM_011537103.1:c.820_823delinsGAGC	XP_011535405.1:p.Glu274=
XM_011537104.1:c.859_862delinsGAGC	XP_011535406.1:p.Glu287=
XR_943842.1:n.954-3108_954-3105delinsGCTC
XR_943843.1:n.954-3108_954-3105delinsGCTC
NM_006939.3:c.859_862delinsGAGC	NP_008870.2:p.Glu287=
NM_006939.4:c.859_862delinsGAGC MANE Select	NP_008870.2:p.Glu287=