Canonical Allele Identifier: CA2624771081

Gene: SOS2

Linked Data

• gnomAD v4: 14-50150263-T-TCAAG

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50150263_50150264insCAAG , CM000676.2:g.50150263_50150264insCAAG	GRCh38
NC_000014.8:g.50616981_50616982insCAAG , CM000676.1:g.50616981_50616982insCAAG	GRCh37
NC_000014.7:g.49686731_49686732insCAAG	NCBI36
NG_051073.1:g.86430_86431insCTTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000216373.10:c.2162-34_2162-33insCTTG MANE Select	ENSP00000216373.5:n.2162-34_2162-33insCTT...
ENST00000216373.9:c.2162-34_2162-33insCTTG	ENSP00000216373.5:n.2162-34_2162-33insCTT...
ENST00000543680.5:c.2063-34_2063-33insCTTG	ENSP00000445328.1:n.2063-34_2063-33insCTT...
NM_006939.2:c.2162-34_2162-33insCTTG	NP_008870.2:n.2162-34_2162-33insCTTG
XM_005268021.1:c.1982-34_1982-33insCTTG	XP_005268078.1:n.1982-34_1982-33insCTTG
XM_011537103.1:c.2123-34_2123-33insCTTG	XP_011535405.1:n.2123-34_2123-33insCTTG
XM_011537104.1:c.2162-34_2162-33insCTTG	XP_011535406.1:n.2162-34_2162-33insCTTG
NM_006939.3:c.2162-34_2162-33insCTTG	NP_008870.2:n.2162-34_2162-33insCTTG
NM_006939.4:c.2162-34_2162-33insCTTG MANE Select	NP_008870.2:n.2162-34_2162-33insCTTG