Canonical Allele Identifier: CA2136084865

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180873_50180874delinsGA , CM000676.2:g.50180873_50180874delinsGA	GRCh38
NC_000014.8:g.50647591_50647592delinsGA , CM000676.1:g.50647591_50647592delinsGA	GRCh37
NC_000014.7:g.49717341_49717342delinsGA	NCBI36
NG_051073.1:g.55820_55821delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-192_859-191delinsTC MANE Select	ENSP00000216373.5:n.859-192_859-191delinsTC
ENST00000216373.9:c.859-192_859-191delinsTC	ENSP00000216373.5:n.859-192_859-191delinsTC
ENST00000543680.5:c.859-192_859-191delinsTC	ENSP00000445328.1:n.859-192_859-191delinsTC
NM_006939.2:c.859-192_859-191delinsTC	NP_008870.2:n.859-192_859-191delinsTC
XM_005268021.1:c.679-192_679-191delinsTC	XP_005268078.1:n.679-192_679-191delinsTC
XM_011537103.1:c.820-192_820-191delinsTC	XP_011535405.1:n.820-192_820-191delinsTC
XM_011537104.1:c.859-192_859-191delinsTC	XP_011535406.1:n.859-192_859-191delinsTC
XR_943842.1:n.954-2914_954-2913delinsGA
XR_943843.1:n.954-2914_954-2913delinsGA
NM_006939.3:c.859-192_859-191delinsTC	NP_008870.2:n.859-192_859-191delinsTC
NM_006939.4:c.859-192_859-191delinsTC MANE Select	NP_008870.2:n.859-192_859-191delinsTC