Canonical Allele Identifier: CA2136086374

Gene: SOS2

Linked Data

• dbSNP Id: rs1885773825

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50182422_50182440del , CM000676.2:g.50182422_50182440del	GRCh38
NC_000014.8:g.50649140_50649158del , CM000676.1:g.50649140_50649158del	GRCh37
NC_000014.7:g.49718890_49718908del	NCBI36
NG_051073.1:g.54256_54274del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.858+25_858+43del MANE Select	ENSP00000216373.5:n.858+25_858+43del
ENST00000216373.9:c.858+25_858+43del	ENSP00000216373.5:n.858+25_858+43del
ENST00000543680.5:c.858+25_858+43del	ENSP00000445328.1:n.858+25_858+43del
NM_006939.2:c.858+25_858+43del	NP_008870.2:n.858+25_858+43del
XM_005268021.1:c.678+25_678+43del	XP_005268078.1:n.678+25_678+43del
XM_011537103.1:c.819+25_819+43del	XP_011535405.1:n.819+25_819+43del
XM_011537104.1:c.858+25_858+43del	XP_011535406.1:n.858+25_858+43del
XR_943842.1:n.954-1365_954-1347del
XR_943843.1:n.954-1365_954-1347del
NM_006939.3:c.858+25_858+43del	NP_008870.2:n.858+25_858+43del
NM_006939.4:c.858+25_858+43del MANE Select	NP_008870.2:n.858+25_858+43del