Canonical Allele Identifier: CA2136086381

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50182424_50182426delinsAGG , CM000676.2:g.50182424_50182426delinsAGG	GRCh38
NC_000014.8:g.50649142_50649144delinsAGG , CM000676.1:g.50649142_50649144delinsAGG	GRCh37
NC_000014.7:g.49718892_49718894delinsAGG	NCBI36
NG_051073.1:g.54268_54270delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.858+37_858+39delinsCCT MANE Select	ENSP00000216373.5:n.858+37_858+39delinsCCT
ENST00000216373.9:c.858+37_858+39delinsCCT	ENSP00000216373.5:n.858+37_858+39delinsCCT
ENST00000543680.5:c.858+37_858+39delinsCCT	ENSP00000445328.1:n.858+37_858+39delinsCCT
NM_006939.2:c.858+37_858+39delinsCCT	NP_008870.2:n.858+37_858+39delinsCCT
XM_005268021.1:c.678+37_678+39delinsCCT	XP_005268078.1:n.678+37_678+39delinsCCT
XM_011537103.1:c.819+37_819+39delinsCCT	XP_011535405.1:n.819+37_819+39delinsCCT
XM_011537104.1:c.858+37_858+39delinsCCT	XP_011535406.1:n.858+37_858+39delinsCCT
XR_943842.1:n.954-1363_954-1361delinsAGG
XR_943843.1:n.954-1363_954-1361delinsAGG
NM_006939.3:c.858+37_858+39delinsCCT	NP_008870.2:n.858+37_858+39delinsCCT
NM_006939.4:c.858+37_858+39delinsCCT MANE Select	NP_008870.2:n.858+37_858+39delinsCCT