Canonical Allele Identifier: CA486175294

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50157067T>C , CM000676.2:g.50157067T>C	GRCh38
NC_000014.8:g.50623785T>C , CM000676.1:g.50623785T>C	GRCh37
NC_000014.7:g.49693535T>C	NCBI36
NG_051073.1:g.79627A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006939.4:c.1989A>G MANE Select	NP_008870.2:p.Lys663=
ENST00000216373.10:c.1989A>G MANE Select	ENSP00000216373.5:p.Lys663=
NM_006939.2:c.1989A>G	NP_008870.2:p.Lys663=
NM_006939.3:c.1989A>G	NP_008870.2:p.Lys663=
ENST00000216373.9:c.1989A>G	ENSP00000216373.5:p.Lys663=
ENST00000543680.5:c.1890A>G	ENSP00000445328.1:p.Lys630=
ENST00000555794.2:c.1103A>G
XM_005268021.1:c.1809A>G	XP_005268078.1:p.Lys603=
XM_011537103.1:c.1950A>G	XP_011535405.1:p.Lys650=
XM_011537104.1:c.1989A>G	XP_011535406.1:p.Lys663=