Canonical Allele Identifier: CA2136084838

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180847_50180848delinsGA , CM000676.2:g.50180847_50180848delinsGA	GRCh38
NC_000014.8:g.50647565_50647566delinsGA , CM000676.1:g.50647565_50647566delinsGA	GRCh37
NC_000014.7:g.49717315_49717316delinsGA	NCBI36
NG_051073.1:g.55846_55847delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-166_859-165delinsTC MANE Select	ENSP00000216373.5:n.859-166_859-165delinsTC
ENST00000216373.9:c.859-166_859-165delinsTC	ENSP00000216373.5:n.859-166_859-165delinsTC
ENST00000543680.5:c.859-166_859-165delinsTC	ENSP00000445328.1:n.859-166_859-165delinsTC
NM_006939.2:c.859-166_859-165delinsTC	NP_008870.2:n.859-166_859-165delinsTC
XM_005268021.1:c.679-166_679-165delinsTC	XP_005268078.1:n.679-166_679-165delinsTC
XM_011537103.1:c.820-166_820-165delinsTC	XP_011535405.1:n.820-166_820-165delinsTC
XM_011537104.1:c.859-166_859-165delinsTC	XP_011535406.1:n.859-166_859-165delinsTC
XR_943842.1:n.954-2940_954-2939delinsGA
XR_943843.1:n.954-2940_954-2939delinsGA
NM_006939.3:c.859-166_859-165delinsTC	NP_008870.2:n.859-166_859-165delinsTC
NM_006939.4:c.859-166_859-165delinsTC MANE Select	NP_008870.2:n.859-166_859-165delinsTC