Canonical Allele Identifier: CA2136084698

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180696_50180698delinsAAG , CM000676.2:g.50180696_50180698delinsAAG	GRCh38
NC_000014.8:g.50647414_50647416delinsAAG , CM000676.1:g.50647414_50647416delinsAAG	GRCh37
NC_000014.7:g.49717164_49717166delinsAAG	NCBI36
NG_051073.1:g.55996_55998delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-16_859-14delinsCTT MANE Select	ENSP00000216373.5:n.859-16_859-14delinsCTT
ENST00000216373.9:c.859-16_859-14delinsCTT	ENSP00000216373.5:n.859-16_859-14delinsCTT
ENST00000543680.5:c.859-16_859-14delinsCTT	ENSP00000445328.1:n.859-16_859-14delinsCTT
NM_006939.2:c.859-16_859-14delinsCTT	NP_008870.2:n.859-16_859-14delinsCTT
XM_005268021.1:c.679-16_679-14delinsCTT	XP_005268078.1:n.679-16_679-14delinsCTT
XM_011537103.1:c.820-16_820-14delinsCTT	XP_011535405.1:n.820-16_820-14delinsCTT
XM_011537104.1:c.859-16_859-14delinsCTT	XP_011535406.1:n.859-16_859-14delinsCTT
XR_943842.1:n.954-3091_954-3089delinsAAG
XR_943843.1:n.954-3091_954-3089delinsAAG
NM_006939.3:c.859-16_859-14delinsCTT	NP_008870.2:n.859-16_859-14delinsCTT
NM_006939.4:c.859-16_859-14delinsCTT MANE Select	NP_008870.2:n.859-16_859-14delinsCTT