Canonical Allele Identifier: CA389647137

Gene: SOS2

Linked Data

• COSMIC: COSM296959 ; COSM296960
• MyVariant Identifiers: chr14:g.50647396T>C (hg19) ; chr14:g.50180678T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180678T>C , CM000676.2:g.50180678T>C	GRCh38
NC_000014.8:g.50647396T>C , CM000676.1:g.50647396T>C	GRCh37
NC_000014.7:g.49717146T>C	NCBI36
NG_051073.1:g.56016A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.863A>G MANE Select	ENSP00000216373.5:p.Gln288Arg
ENST00000216373.9:c.863A>G	ENSP00000216373.5:p.Gln288Arg
ENST00000543680.5:c.863A>G	ENSP00000445328.1:p.Gln288Arg
NM_006939.2:c.863A>G	NP_008870.2:p.Gln288Arg
XM_005268021.1:c.683A>G	XP_005268078.1:p.Gln228Arg
XM_011537103.1:c.824A>G	XP_011535405.1:p.Gln275Arg
XM_011537104.1:c.863A>G	XP_011535406.1:p.Gln288Arg
XR_943842.1:n.954-3109T>C
XR_943843.1:n.954-3109T>C
NM_006939.3:c.863A>G	NP_008870.2:p.Gln288Arg
NM_006939.4:c.863A>G MANE Select	NP_008870.2:p.Gln288Arg