Canonical Allele Identifier: CA2136084882
Gene: SOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50180878_50180881delinsGAGA , CM000676.2:g.50180878_50180881delinsGAGA GRCh38
NC_000014.8:g.50647596_50647599delinsGAGA , CM000676.1:g.50647596_50647599delinsGAGA GRCh37
NC_000014.7:g.49717346_49717349delinsGAGA NCBI36
NG_051073.1:g.55813_55816delinsTCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000216373.10:c.859-199_859-196delinsTCTC MANE Select ENSP00000216373.5:n.859-199_859-196delinsTCTC
ENST00000216373.9:c.859-199_859-196delinsTCTC ENSP00000216373.5:n.859-199_859-196delinsTCTC
ENST00000543680.5:c.859-199_859-196delinsTCTC ENSP00000445328.1:n.859-199_859-196delinsTCTC
NM_006939.2:c.859-199_859-196delinsTCTC NP_008870.2:n.859-199_859-196delinsTCTC
XM_005268021.1:c.679-199_679-196delinsTCTC XP_005268078.1:n.679-199_679-196delinsTCTC
XM_011537103.1:c.820-199_820-196delinsTCTC XP_011535405.1:n.820-199_820-196delinsTCTC
XM_011537104.1:c.859-199_859-196delinsTCTC XP_011535406.1:n.859-199_859-196delinsTCTC
XR_943842.1:n.954-2909_954-2906delinsGAGA
XR_943843.1:n.954-2909_954-2906delinsGAGA
NM_006939.3:c.859-199_859-196delinsTCTC NP_008870.2:n.859-199_859-196delinsTCTC
NM_006939.4:c.859-199_859-196delinsTCTC MANE Select NP_008870.2:n.859-199_859-196delinsTCTC