Canonical Allele Identifier: CA2136084748

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180747_50180748delinsAG , CM000676.2:g.50180747_50180748delinsAG	GRCh38
NC_000014.8:g.50647465_50647466delinsAG , CM000676.1:g.50647465_50647466delinsAG	GRCh37
NC_000014.7:g.49717215_49717216delinsAG	NCBI36
NG_051073.1:g.55946_55947delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-66_859-65delinsCT MANE Select	ENSP00000216373.5:n.859-66_859-65delinsCT
ENST00000216373.9:c.859-66_859-65delinsCT	ENSP00000216373.5:n.859-66_859-65delinsCT
ENST00000543680.5:c.859-66_859-65delinsCT	ENSP00000445328.1:n.859-66_859-65delinsCT
NM_006939.2:c.859-66_859-65delinsCT	NP_008870.2:n.859-66_859-65delinsCT
XM_005268021.1:c.679-66_679-65delinsCT	XP_005268078.1:n.679-66_679-65delinsCT
XM_011537103.1:c.820-66_820-65delinsCT	XP_011535405.1:n.820-66_820-65delinsCT
XM_011537104.1:c.859-66_859-65delinsCT	XP_011535406.1:n.859-66_859-65delinsCT
XR_943842.1:n.954-3040_954-3039delinsAG
XR_943843.1:n.954-3040_954-3039delinsAG
NM_006939.3:c.859-66_859-65delinsCT	NP_008870.2:n.859-66_859-65delinsCT
NM_006939.4:c.859-66_859-65delinsCT MANE Select	NP_008870.2:n.859-66_859-65delinsCT