Canonical Allele Identifier: CA2136086436
Gene: SOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50182504G= , CM000676.2:g.50182504G= GRCh38
NC_000014.8:g.50649222G= , CM000676.1:g.50649222G= GRCh37
NC_000014.7:g.49718972G= NCBI36
NG_051073.1:g.54190C=

Transcript Alleles

HGVS Amino-acid change
ENST00000216373.10:c.817C= MANE Select ENSP00000216373.5:p.Pro273=
ENST00000216373.9:c.817C= ENSP00000216373.5:p.Pro273=
ENST00000543680.5:c.817C= ENSP00000445328.1:p.Pro273=
ENST00000556469.5:n.584C=
NM_006939.2:c.817C= NP_008870.2:p.Pro273=
XM_005268021.1:c.637C= XP_005268078.1:p.Pro213=
XM_011537103.1:c.778C= XP_011535405.1:p.Pro260=
XM_011537104.1:c.817C= XP_011535406.1:p.Pro273=
XR_943842.1:n.954-1283G=
XR_943843.1:n.954-1283G=
NM_006939.3:c.817C= NP_008870.2:p.Pro273=
NM_006939.4:c.817C= MANE Select NP_008870.2:p.Pro273=