Canonical Allele Identifier: CA2624772530

Gene: SOS2

Linked Data

• gnomAD v4: 14-50180727-A-AACAAAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180727_50180728insACAAAGG , CM000676.2:g.50180727_50180728insACAAAGG	GRCh38
NC_000014.8:g.50647445_50647446insACAAAGG , CM000676.1:g.50647445_50647446insACAAAGG	GRCh37
NC_000014.7:g.49717195_49717196insACAAAGG	NCBI36
NG_051073.1:g.55966_55967insCCTTTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-46_859-45insCCTTTGT MANE Select	ENSP00000216373.5:n.859-46_859-45insCCTTTGT
ENST00000216373.9:c.859-46_859-45insCCTTTGT	ENSP00000216373.5:n.859-46_859-45insCCTTTGT
ENST00000543680.5:c.859-46_859-45insCCTTTGT	ENSP00000445328.1:n.859-46_859-45insCCTTTGT
NM_006939.2:c.859-46_859-45insCCTTTGT	NP_008870.2:n.859-46_859-45insCCTTTGT
XM_005268021.1:c.679-46_679-45insCCTTTGT	XP_005268078.1:n.679-46_679-45insCCTTTGT
XM_011537103.1:c.820-46_820-45insCCTTTGT	XP_011535405.1:n.820-46_820-45insCCTTTGT
XM_011537104.1:c.859-46_859-45insCCTTTGT	XP_011535406.1:n.859-46_859-45insCCTTTGT
XR_943842.1:n.954-3060_954-3059insACAAAGG
XR_943843.1:n.954-3060_954-3059insACAAAGG
NM_006939.3:c.859-46_859-45insCCTTTGT	NP_008870.2:n.859-46_859-45insCCTTTGT
NM_006939.4:c.859-46_859-45insCCTTTGT MANE Select	NP_008870.2:n.859-46_859-45insCCTTTGT