Canonical Allele Identifier: CA2624771481

Gene: SOS2

Linked Data

• gnomAD v4: 14-50153136-AATG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50153140_50153142del , CM000676.2:g.50153140_50153142del	GRCh38
NC_000014.8:g.50619858_50619860del , CM000676.1:g.50619858_50619860del	GRCh37
NC_000014.7:g.49689608_49689610del	NCBI36
NG_051073.1:g.83555_83557del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.2092_2094del MANE Select	ENSP00000216373.5:p.His698del
ENST00000216373.9:c.2092_2094del	ENSP00000216373.5:p.His698del
ENST00000543680.5:c.1993_1995del	ENSP00000445328.1:p.His665del
NM_006939.2:c.2092_2094del	NP_008870.2:p.His698del
XM_005268021.1:c.1912_1914del	XP_005268078.1:p.His638del
XM_011537103.1:c.2053_2055del	XP_011535405.1:p.His685del
XM_011537104.1:c.2092_2094del	XP_011535406.1:p.His698del
NM_006939.3:c.2092_2094del	NP_008870.2:p.His698del
NM_006939.4:c.2092_2094del MANE Select	NP_008870.2:p.His698del