Canonical Allele Identifier: CA260706937

Gene: SOS2

Linked Data

• dbSNP Id: rs922603472
• gnomAD v3: 14-50180878-GAGA-G
• gnomAD v4: 14-50180878-GAGA-G
• MyVariant Identifiers: chr14:g.50647597_50647599del (hg19) ; chr14:g.50180879_50180881del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180886_50180888del , CM000676.2:g.50180886_50180888del	GRCh38
NC_000014.8:g.50647604_50647606del , CM000676.1:g.50647604_50647606del	GRCh37
NC_000014.7:g.49717354_49717356del	NCBI36
NG_051073.1:g.55813_55815del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-199_859-197del MANE Select	ENSP00000216373.5:n.859-199_859-197del
ENST00000216373.9:c.859-199_859-197del	ENSP00000216373.5:n.859-199_859-197del
ENST00000543680.5:c.859-199_859-197del	ENSP00000445328.1:n.859-199_859-197del
NM_006939.2:c.859-199_859-197del	NP_008870.2:n.859-199_859-197del
XM_005268021.1:c.679-199_679-197del	XP_005268078.1:n.679-199_679-197del
XM_011537103.1:c.820-199_820-197del	XP_011535405.1:n.820-199_820-197del
XM_011537104.1:c.859-199_859-197del	XP_011535406.1:n.859-199_859-197del
XR_943842.1:n.954-2901_954-2899del
XR_943843.1:n.954-2901_954-2899del
NM_006939.3:c.859-199_859-197del	NP_008870.2:n.859-199_859-197del
NM_006939.4:c.859-199_859-197del MANE Select	NP_008870.2:n.859-199_859-197del