Canonical Allele Identifier: CA2516422805

Gene: SOS2

Linked Data

• gnomAD v4: 14-50180685-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180692dup , CM000676.2:g.50180692dup	GRCh38
NC_000014.8:g.50647410dup , CM000676.1:g.50647410dup	GRCh37
NC_000014.7:g.49717160dup	NCBI36
NG_051073.1:g.56008dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-4dup MANE Select	ENSP00000216373.5:n.859-4dup
ENST00000216373.9:c.859-4dup	ENSP00000216373.5:n.859-4dup
ENST00000543680.5:c.859-4dup	ENSP00000445328.1:n.859-4dup
NM_006939.2:c.859-4dup	NP_008870.2:n.859-4dup
XM_005268021.1:c.679-4dup	XP_005268078.1:n.679-4dup
XM_011537103.1:c.820-4dup	XP_011535405.1:n.820-4dup
XM_011537104.1:c.859-4dup	XP_011535406.1:n.859-4dup
XR_943842.1:n.954-3095dup
XR_943843.1:n.954-3095dup
NM_006939.3:c.859-4dup	NP_008870.2:n.859-4dup
NM_006939.4:c.859-4dup MANE Select	NP_008870.2:n.859-4dup