Canonical Allele Identifier: CA2136084688

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180685_50180686delinsAT , CM000676.2:g.50180685_50180686delinsAT	GRCh38
NC_000014.8:g.50647403_50647404delinsAT , CM000676.1:g.50647403_50647404delinsAT	GRCh37
NC_000014.7:g.49717153_49717154delinsAT	NCBI36
NG_051073.1:g.56008_56009delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-4_859-3delinsAT MANE Select	ENSP00000216373.5:n.859-4_859-3delinsAT
ENST00000216373.9:c.859-4_859-3delinsAT	ENSP00000216373.5:n.859-4_859-3delinsAT
ENST00000543680.5:c.859-4_859-3delinsAT	ENSP00000445328.1:n.859-4_859-3delinsAT
NM_006939.2:c.859-4_859-3delinsAT	NP_008870.2:n.859-4_859-3delinsAT
XM_005268021.1:c.679-4_679-3delinsAT	XP_005268078.1:n.679-4_679-3delinsAT
XM_011537103.1:c.820-4_820-3delinsAT	XP_011535405.1:n.820-4_820-3delinsAT
XM_011537104.1:c.859-4_859-3delinsAT	XP_011535406.1:n.859-4_859-3delinsAT
XR_943842.1:n.954-3102_954-3101delinsAT
XR_943843.1:n.954-3102_954-3101delinsAT
NM_006939.3:c.859-4_859-3delinsAT	NP_008870.2:n.859-4_859-3delinsAT
NM_006939.4:c.859-4_859-3delinsAT MANE Select	NP_008870.2:n.859-4_859-3delinsAT