Canonical Allele Identifier: CA2136084880

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180877_50180880delinsAGAG , CM000676.2:g.50180877_50180880delinsAGAG	GRCh38
NC_000014.8:g.50647595_50647598delinsAGAG , CM000676.1:g.50647595_50647598delinsAGAG	GRCh37
NC_000014.7:g.49717345_49717348delinsAGAG	NCBI36
NG_051073.1:g.55814_55817delinsCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-198_859-195delinsCTCT MANE Select	ENSP00000216373.5:n.859-198_859-195delinsCTCT
ENST00000216373.9:c.859-198_859-195delinsCTCT	ENSP00000216373.5:n.859-198_859-195delinsCTCT
ENST00000543680.5:c.859-198_859-195delinsCTCT	ENSP00000445328.1:n.859-198_859-195delinsCTCT
NM_006939.2:c.859-198_859-195delinsCTCT	NP_008870.2:n.859-198_859-195delinsCTCT
XM_005268021.1:c.679-198_679-195delinsCTCT	XP_005268078.1:n.679-198_679-195delinsCTCT
XM_011537103.1:c.820-198_820-195delinsCTCT	XP_011535405.1:n.820-198_820-195delinsCTCT
XM_011537104.1:c.859-198_859-195delinsCTCT	XP_011535406.1:n.859-198_859-195delinsCTCT
XR_943842.1:n.954-2910_954-2907delinsAGAG
XR_943843.1:n.954-2910_954-2907delinsAGAG
NM_006939.3:c.859-198_859-195delinsCTCT	NP_008870.2:n.859-198_859-195delinsCTCT
NM_006939.4:c.859-198_859-195delinsCTCT MANE Select	NP_008870.2:n.859-198_859-195delinsCTCT