Canonical Allele Identifier: CA2575520449

Gene: SOS2

Linked Data

• gnomAD v4: 14-50153022-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50153025del , CM000676.2:g.50153025del	GRCh38
NC_000014.8:g.50619743del , CM000676.1:g.50619743del	GRCh37
NC_000014.7:g.49689493del	NCBI36
NG_051073.1:g.83671del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.2161+47del MANE Select	ENSP00000216373.5:n.2161+47del
ENST00000216373.9:c.2161+47del	ENSP00000216373.5:n.2161+47del
ENST00000543680.5:c.2062+47del	ENSP00000445328.1:n.2062+47del
NM_006939.2:c.2161+47del	NP_008870.2:n.2161+47del
XM_005268021.1:c.1981+47del	XP_005268078.1:n.1981+47del
XM_011537103.1:c.2122+47del	XP_011535405.1:n.2122+47del
XM_011537104.1:c.2161+47del	XP_011535406.1:n.2161+47del
NM_006939.3:c.2161+47del	NP_008870.2:n.2161+47del
NM_006939.4:c.2161+47del MANE Select	NP_008870.2:n.2161+47del