Canonical Allele Identifier: CA919415827

Gene: SOS2

Linked Data

• dbSNP Id: rs1594999990

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180873_50180875del , CM000676.2:g.50180873_50180875del	GRCh38
NC_000014.8:g.50647591_50647593del , CM000676.1:g.50647591_50647593del	GRCh37
NC_000014.7:g.49717341_49717343del	NCBI36
NG_051073.1:g.55819_55821del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-193_859-191del MANE Select	ENSP00000216373.5:n.859-193_859-191del
ENST00000216373.9:c.859-193_859-191del	ENSP00000216373.5:n.859-193_859-191del
ENST00000543680.5:c.859-193_859-191del	ENSP00000445328.1:n.859-193_859-191del
NM_006939.2:c.859-193_859-191del	NP_008870.2:n.859-193_859-191del
XM_005268021.1:c.679-193_679-191del	XP_005268078.1:n.679-193_679-191del
XM_011537103.1:c.820-193_820-191del	XP_011535405.1:n.820-193_820-191del
XM_011537104.1:c.859-193_859-191del	XP_011535406.1:n.859-193_859-191del
XR_943842.1:n.954-2914_954-2912del
XR_943843.1:n.954-2914_954-2912del
NM_006939.3:c.859-193_859-191del	NP_008870.2:n.859-193_859-191del
NM_006939.4:c.859-193_859-191del MANE Select	NP_008870.2:n.859-193_859-191del