Canonical Allele Identifier: CA2136066057

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50153058_50153063delinsTATATA , CM000676.2:g.50153058_50153063delinsTATATA	GRCh38
NC_000014.8:g.50619776_50619781delinsTATATA , CM000676.1:g.50619776_50619781delinsTATATA	GRCh37
NC_000014.7:g.49689526_49689531delinsTATATA	NCBI36
NG_051073.1:g.83631_83636delinsTATATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.2161+7_2161+12delinsTATATA MANE Select	ENSP00000216373.5:n.2161+7_2161+12delinsTATATA
ENST00000216373.9:c.2161+7_2161+12delinsTATATA	ENSP00000216373.5:n.2161+7_2161+12delinsTATATA
ENST00000543680.5:c.2062+7_2062+12delinsTATATA	ENSP00000445328.1:n.2062+7_2062+12delinsTATATA
NM_006939.2:c.2161+7_2161+12delinsTATATA	NP_008870.2:n.2161+7_2161+12delinsTATATA
XM_005268021.1:c.1981+7_1981+12delinsTATATA	XP_005268078.1:n.1981+7_1981+12delinsTATATA
XM_011537103.1:c.2122+7_2122+12delinsTATATA	XP_011535405.1:n.2122+7_2122+12delinsTATATA
XM_011537104.1:c.2161+7_2161+12delinsTATATA	XP_011535406.1:n.2161+7_2161+12delinsTATATA
NM_006939.3:c.2161+7_2161+12delinsTATATA	NP_008870.2:n.2161+7_2161+12delinsTATATA
NM_006939.4:c.2161+7_2161+12delinsTATATA MANE Select	NP_008870.2:n.2161+7_2161+12delinsTATATA