Canonical Allele Identifier: CA2136084858

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180870_50180875delinsAAAGAG , CM000676.2:g.50180870_50180875delinsAAAGAG	GRCh38
NC_000014.8:g.50647588_50647593delinsAAAGAG , CM000676.1:g.50647588_50647593delinsAAAGAG	GRCh37
NC_000014.7:g.49717338_49717343delinsAAAGAG	NCBI36
NG_051073.1:g.55819_55824delinsCTCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-193_859-188delinsCTCTTT MANE Select	ENSP00000216373.5:n.859-193_859-188delinsCTCTTT
ENST00000216373.9:c.859-193_859-188delinsCTCTTT	ENSP00000216373.5:n.859-193_859-188delinsCTCTTT
ENST00000543680.5:c.859-193_859-188delinsCTCTTT	ENSP00000445328.1:n.859-193_859-188delinsCTCTTT
NM_006939.2:c.859-193_859-188delinsCTCTTT	NP_008870.2:n.859-193_859-188delinsCTCTTT
XM_005268021.1:c.679-193_679-188delinsCTCTTT	XP_005268078.1:n.679-193_679-188delinsCTCTTT
XM_011537103.1:c.820-193_820-188delinsCTCTTT	XP_011535405.1:n.820-193_820-188delinsCTCTTT
XM_011537104.1:c.859-193_859-188delinsCTCTTT	XP_011535406.1:n.859-193_859-188delinsCTCTTT
XR_943842.1:n.954-2917_954-2912delinsAAAGAG
XR_943843.1:n.954-2917_954-2912delinsAAAGAG
NM_006939.3:c.859-193_859-188delinsCTCTTT	NP_008870.2:n.859-193_859-188delinsCTCTTT
NM_006939.4:c.859-193_859-188delinsCTCTTT MANE Select	NP_008870.2:n.859-193_859-188delinsCTCTTT