Canonical Allele Identifier: CA2136084851

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180861_50180862delinsGA , CM000676.2:g.50180861_50180862delinsGA	GRCh38
NC_000014.8:g.50647579_50647580delinsGA , CM000676.1:g.50647579_50647580delinsGA	GRCh37
NC_000014.7:g.49717329_49717330delinsGA	NCBI36
NG_051073.1:g.55832_55833delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-180_859-179delinsTC MANE Select	ENSP00000216373.5:n.859-180_859-179delinsTC
ENST00000216373.9:c.859-180_859-179delinsTC	ENSP00000216373.5:n.859-180_859-179delinsTC
ENST00000543680.5:c.859-180_859-179delinsTC	ENSP00000445328.1:n.859-180_859-179delinsTC
NM_006939.2:c.859-180_859-179delinsTC	NP_008870.2:n.859-180_859-179delinsTC
XM_005268021.1:c.679-180_679-179delinsTC	XP_005268078.1:n.679-180_679-179delinsTC
XM_011537103.1:c.820-180_820-179delinsTC	XP_011535405.1:n.820-180_820-179delinsTC
XM_011537104.1:c.859-180_859-179delinsTC	XP_011535406.1:n.859-180_859-179delinsTC
XR_943842.1:n.954-2926_954-2925delinsGA
XR_943843.1:n.954-2926_954-2925delinsGA
NM_006939.3:c.859-180_859-179delinsTC	NP_008870.2:n.859-180_859-179delinsTC
NM_006939.4:c.859-180_859-179delinsTC MANE Select	NP_008870.2:n.859-180_859-179delinsTC