Canonical Allele Identifier: CA2136084859

Gene: SOS2

Linked Data

• dbSNP Id: rs1885710803
• gnomAD v3: 14-50180870-AAAGAG-A
• gnomAD v4: 14-50180870-AAAGAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180880_50180884del , CM000676.2:g.50180880_50180884del	GRCh38
NC_000014.8:g.50647598_50647602del , CM000676.1:g.50647598_50647602del	GRCh37
NC_000014.7:g.49717348_49717352del	NCBI36
NG_051073.1:g.55819_55823del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-193_859-189del MANE Select	ENSP00000216373.5:n.859-193_859-189del
ENST00000216373.9:c.859-193_859-189del	ENSP00000216373.5:n.859-193_859-189del
ENST00000543680.5:c.859-193_859-189del	ENSP00000445328.1:n.859-193_859-189del
NM_006939.2:c.859-193_859-189del	NP_008870.2:n.859-193_859-189del
XM_005268021.1:c.679-193_679-189del	XP_005268078.1:n.679-193_679-189del
XM_011537103.1:c.820-193_820-189del	XP_011535405.1:n.820-193_820-189del
XM_011537104.1:c.859-193_859-189del	XP_011535406.1:n.859-193_859-189del
XR_943842.1:n.954-2907_954-2903del
XR_943843.1:n.954-2907_954-2903del
NM_006939.3:c.859-193_859-189del	NP_008870.2:n.859-193_859-189del
NM_006939.4:c.859-193_859-189del MANE Select	NP_008870.2:n.859-193_859-189del