Canonical Allele Identifier: CA389647057
Gene: SOS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50180644G>T , CM000676.2:g.50180644G>T GRCh38
NC_000014.8:g.50647362G>T , CM000676.1:g.50647362G>T GRCh37
NC_000014.7:g.49717112G>T NCBI36
NG_051073.1:g.56050C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000216373.10:c.897C>A MANE Select ENSP00000216373.5:p.Asp299Glu
ENST00000216373.9:c.897C>A ENSP00000216373.5:p.Asp299Glu
ENST00000543680.5:c.897C>A ENSP00000445328.1:p.Asp299Glu
ENST00000555794.2:c.11C>A
NM_006939.2:c.897C>A NP_008870.2:p.Asp299Glu
XM_005268021.1:c.717C>A XP_005268078.1:p.Asp239Glu
XM_011537103.1:c.858C>A XP_011535405.1:p.Asp286Glu
XM_011537104.1:c.897C>A XP_011535406.1:p.Asp299Glu
XR_943842.1:n.954-3143G>T
XR_943843.1:n.954-3143G>T
NM_006939.3:c.897C>A NP_008870.2:p.Asp299Glu
NM_006939.4:c.897C>A MANE Select NP_008870.2:p.Asp299Glu