Canonical Allele Identifier: CA2136084840

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180848_50180852delinsAAAAG , CM000676.2:g.50180848_50180852delinsAAAAG	GRCh38
NC_000014.8:g.50647566_50647570delinsAAAAG , CM000676.1:g.50647566_50647570delinsAAAAG	GRCh37
NC_000014.7:g.49717316_49717320delinsAAAAG	NCBI36
NG_051073.1:g.55842_55846delinsCTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-170_859-166delinsCTTTT MANE Select	ENSP00000216373.5:n.859-170_859-166delinsCTTTT
ENST00000216373.9:c.859-170_859-166delinsCTTTT	ENSP00000216373.5:n.859-170_859-166delinsCTTTT
ENST00000543680.5:c.859-170_859-166delinsCTTTT	ENSP00000445328.1:n.859-170_859-166delinsCTTTT
NM_006939.2:c.859-170_859-166delinsCTTTT	NP_008870.2:n.859-170_859-166delinsCTTTT
XM_005268021.1:c.679-170_679-166delinsCTTTT	XP_005268078.1:n.679-170_679-166delinsCTTTT
XM_011537103.1:c.820-170_820-166delinsCTTTT	XP_011535405.1:n.820-170_820-166delinsCTTTT
XM_011537104.1:c.859-170_859-166delinsCTTTT	XP_011535406.1:n.859-170_859-166delinsCTTTT
XR_943842.1:n.954-2939_954-2935delinsAAAAG
XR_943843.1:n.954-2939_954-2935delinsAAAAG
NM_006939.3:c.859-170_859-166delinsCTTTT	NP_008870.2:n.859-170_859-166delinsCTTTT
NM_006939.4:c.859-170_859-166delinsCTTTT MANE Select	NP_008870.2:n.859-170_859-166delinsCTTTT