Canonical Allele Identifier: CA2136058838

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50130600_50130602delinsCTG , CM000676.2:g.50130600_50130602delinsCTG	GRCh38
NC_000014.8:g.50597318_50597320delinsCTG , CM000676.1:g.50597318_50597320delinsCTG	GRCh37
NC_000014.7:g.49667068_49667070delinsCTG	NCBI36
NG_051073.1:g.106092_106094delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.3236_3238delinsCAG MANE Select	ENSP00000216373.5:p.Thr1079=
ENST00000216373.9:c.3236_3238delinsCAG	ENSP00000216373.5:p.Thr1079=
ENST00000543680.5:c.3137_3139delinsCAG	ENSP00000445328.1:p.Thr1046=
NM_006939.2:c.3236_3238delinsCAG	NP_008870.2:p.Thr1079=
XM_005268021.1:c.3056_3058delinsCAG	XP_005268078.1:p.Thr1019=
XM_011537103.1:c.3197_3199delinsCAG	XP_011535405.1:p.Thr1066=
NM_006939.3:c.3236_3238delinsCAG	NP_008870.2:p.Thr1079=
NM_006939.4:c.3236_3238delinsCAG MANE Select	NP_008870.2:p.Thr1079=