Canonical Allele Identifier: CA2136066019

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50152974_50152977delinsAAAG , CM000676.2:g.50152974_50152977delinsAAAG	GRCh38
NC_000014.8:g.50619692_50619695delinsAAAG , CM000676.1:g.50619692_50619695delinsAAAG	GRCh37
NC_000014.7:g.49689442_49689445delinsAAAG	NCBI36
NG_051073.1:g.83717_83720delinsCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.2161+93_2161+96delinsCTTT MANE Select	ENSP00000216373.5:n.2161+93_2161+96delinsCTTT
ENST00000216373.9:c.2161+93_2161+96delinsCTTT	ENSP00000216373.5:n.2161+93_2161+96delinsCTTT
ENST00000543680.5:c.2062+93_2062+96delinsCTTT	ENSP00000445328.1:n.2062+93_2062+96delinsCTTT
NM_006939.2:c.2161+93_2161+96delinsCTTT	NP_008870.2:n.2161+93_2161+96delinsCTTT
XM_005268021.1:c.1981+93_1981+96delinsCTTT	XP_005268078.1:n.1981+93_1981+96delinsCTTT
XM_011537103.1:c.2122+93_2122+96delinsCTTT	XP_011535405.1:n.2122+93_2122+96delinsCTTT
XM_011537104.1:c.2161+93_2161+96delinsCTTT	XP_011535406.1:n.2161+93_2161+96delinsCTTT
NM_006939.3:c.2161+93_2161+96delinsCTTT	NP_008870.2:n.2161+93_2161+96delinsCTTT
NM_006939.4:c.2161+93_2161+96delinsCTTT MANE Select	NP_008870.2:n.2161+93_2161+96delinsCTTT