Canonical Allele Identifier: CA2801534800

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180808_50180809dup , CM000676.2:g.50180808_50180809dup	GRCh38
NC_000014.8:g.50647526_50647527dup , CM000676.1:g.50647526_50647527dup	GRCh37
NC_000014.7:g.49717276_49717277dup	NCBI36
NG_051073.1:g.55888_55889dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-124_859-123dup MANE Select	ENSP00000216373.5:n.859-124_859-123dup
ENST00000216373.9:c.859-124_859-123dup	ENSP00000216373.5:n.859-124_859-123dup
ENST00000543680.5:c.859-124_859-123dup	ENSP00000445328.1:n.859-124_859-123dup
NM_006939.2:c.859-124_859-123dup	NP_008870.2:n.859-124_859-123dup
XM_005268021.1:c.679-124_679-123dup	XP_005268078.1:n.679-124_679-123dup
XM_011537103.1:c.820-124_820-123dup	XP_011535405.1:n.820-124_820-123dup
XM_011537104.1:c.859-124_859-123dup	XP_011535406.1:n.859-124_859-123dup
XR_943842.1:n.954-2979_954-2978dup
XR_943843.1:n.954-2979_954-2978dup
NM_006939.3:c.859-124_859-123dup	NP_008870.2:n.859-124_859-123dup
NM_006939.4:c.859-124_859-123dup MANE Select	NP_008870.2:n.859-124_859-123dup