Canonical Allele Identifier: CA2575520421

Gene: SOS2

Linked Data

• gnomAD v4: 14-50150241-A-AAC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50150245_50150246dup , CM000676.2:g.50150245_50150246dup	GRCh38
NC_000014.8:g.50616963_50616964dup , CM000676.1:g.50616963_50616964dup	GRCh37
NC_000014.7:g.49686713_49686714dup	NCBI36
NG_051073.1:g.86451_86452dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000216373.10:c.2162-13_2162-12dup MANE Select	ENSP00000216373.5:n.2162-13_2162-12dup
ENST00000216373.9:c.2162-13_2162-12dup	ENSP00000216373.5:n.2162-13_2162-12dup
ENST00000543680.5:c.2063-13_2063-12dup	ENSP00000445328.1:n.2063-13_2063-12dup
NM_006939.2:c.2162-13_2162-12dup	NP_008870.2:n.2162-13_2162-12dup
XM_005268021.1:c.1982-13_1982-12dup	XP_005268078.1:n.1982-13_1982-12dup
XM_011537103.1:c.2123-13_2123-12dup	XP_011535405.1:n.2123-13_2123-12dup
XM_011537104.1:c.2162-13_2162-12dup	XP_011535406.1:n.2162-13_2162-12dup
NM_006939.3:c.2162-13_2162-12dup	NP_008870.2:n.2162-13_2162-12dup
NM_006939.4:c.2162-13_2162-12dup MANE Select	NP_008870.2:n.2162-13_2162-12dup