Canonical Allele Identifier: CA2136084854

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180868_50180873delinsAAAAAG , CM000676.2:g.50180868_50180873delinsAAAAAG	GRCh38
NC_000014.8:g.50647586_50647591delinsAAAAAG , CM000676.1:g.50647586_50647591delinsAAAAAG	GRCh37
NC_000014.7:g.49717336_49717341delinsAAAAAG	NCBI36
NG_051073.1:g.55821_55826delinsCTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-191_859-186delinsCTTTTT MANE Select	ENSP00000216373.5:n.859-191_859-186delinsCTTTTT
ENST00000216373.9:c.859-191_859-186delinsCTTTTT	ENSP00000216373.5:n.859-191_859-186delinsCTTTTT
ENST00000543680.5:c.859-191_859-186delinsCTTTTT	ENSP00000445328.1:n.859-191_859-186delinsCTTTTT
NM_006939.2:c.859-191_859-186delinsCTTTTT	NP_008870.2:n.859-191_859-186delinsCTTTTT
XM_005268021.1:c.679-191_679-186delinsCTTTTT	XP_005268078.1:n.679-191_679-186delinsCTTTTT
XM_011537103.1:c.820-191_820-186delinsCTTTTT	XP_011535405.1:n.820-191_820-186delinsCTTTTT
XM_011537104.1:c.859-191_859-186delinsCTTTTT	XP_011535406.1:n.859-191_859-186delinsCTTTTT
XR_943842.1:n.954-2919_954-2914delinsAAAAAG
XR_943843.1:n.954-2919_954-2914delinsAAAAAG
NM_006939.3:c.859-191_859-186delinsCTTTTT	NP_008870.2:n.859-191_859-186delinsCTTTTT
NM_006939.4:c.859-191_859-186delinsCTTTTT MANE Select	NP_008870.2:n.859-191_859-186delinsCTTTTT