Canonical Allele Identifier: CA2136084400
Gene: SOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50180530_50180534delinsTATTA , CM000676.2:g.50180530_50180534delinsTATTA GRCh38
NC_000014.8:g.50647248_50647252delinsTATTA , CM000676.1:g.50647248_50647252delinsTATTA GRCh37
NC_000014.7:g.49716998_49717002delinsTATTA NCBI36
NG_051073.1:g.56160_56164delinsTAATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000216373.10:c.969+38_969+42delinsTAATA MANE Select ENSP00000216373.5:n.969+38_969+42delinsTAATA
ENST00000216373.9:c.969+38_969+42delinsTAATA ENSP00000216373.5:n.969+38_969+42delinsTAATA
ENST00000543680.5:c.969+38_969+42delinsTAATA ENSP00000445328.1:n.969+38_969+42delinsTAATA
ENST00000555794.2:c.83+38_83+42delinsTAATA
NM_006939.2:c.969+38_969+42delinsTAATA NP_008870.2:n.969+38_969+42delinsTAATA
XM_005268021.1:c.789+38_789+42delinsTAATA XP_005268078.1:n.789+38_789+42delinsTAATA
XM_011537103.1:c.930+38_930+42delinsTAATA XP_011535405.1:n.930+38_930+42delinsTAATA
XM_011537104.1:c.969+38_969+42delinsTAATA XP_011535406.1:n.969+38_969+42delinsTAATA
XR_943842.1:n.954-3257_954-3253delinsTATTA
XR_943843.1:n.954-3257_954-3253delinsTATTA
NM_006939.3:c.969+38_969+42delinsTAATA NP_008870.2:n.969+38_969+42delinsTAATA
NM_006939.4:c.969+38_969+42delinsTAATA MANE Select NP_008870.2:n.969+38_969+42delinsTAATA