Canonical Allele Identifier: CA2624771222

Gene: SOS2

Linked Data

• gnomAD v4: 14-50152955-GCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50152958_50152959del , CM000676.2:g.50152958_50152959del	GRCh38
NC_000014.8:g.50619676_50619677del , CM000676.1:g.50619676_50619677del	GRCh37
NC_000014.7:g.49689426_49689427del	NCBI36
NG_051073.1:g.83737_83738del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.2161+113_2161+114del MANE Select	ENSP00000216373.5:n.2161+113_2161+114del
ENST00000216373.9:c.2161+113_2161+114del	ENSP00000216373.5:n.2161+113_2161+114del
ENST00000543680.5:c.2062+113_2062+114del	ENSP00000445328.1:n.2062+113_2062+114del
NM_006939.2:c.2161+113_2161+114del	NP_008870.2:n.2161+113_2161+114del
XM_005268021.1:c.1981+113_1981+114del	XP_005268078.1:n.1981+113_1981+114del
XM_011537103.1:c.2122+113_2122+114del	XP_011535405.1:n.2122+113_2122+114del
XM_011537104.1:c.2161+113_2161+114del	XP_011535406.1:n.2161+113_2161+114del
NM_006939.3:c.2161+113_2161+114del	NP_008870.2:n.2161+113_2161+114del
NM_006939.4:c.2161+113_2161+114del MANE Select	NP_008870.2:n.2161+113_2161+114del