Canonical Allele Identifier: CA2810020297

Gene: RPS6KB1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.59946921_59946922del , CM000679.2:g.59946921_59946922del	GRCh38
NC_000017.10:g.58024282_58024283del , CM000679.1:g.58024282_58024283del	GRCh37
NC_000017.9:g.55379064_55379065del	NCBI36
NG_029513.1:g.58840_58841del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225577.9:c.*133_*134del MANE Select	ENSP00000225577.4:n.*133_*134del
ENST00000225577.8:c.*133_*134del	ENSP00000225577.4:n.*133_*134del
ENST00000393021.7:c.*133_*134del	ENSP00000376744.3:n.*133_*134del
ENST00000406116.7:c.1341-666_1341-665del	ENSP00000384335.3:n.1341-666_1341-665del
ENST00000443572.6:c.*133_*134del	ENSP00000441993.1:n.*133_*134del
ENST00000472940.5:c.*1746_*1747del	ENSP00000468058.1:n.*1746_*1747del
ENST00000475155.1:n.699_700del
ENST00000591035.1:c.149+1403_149+1404del	ENSP00000468280.1:n.149+1403_149+1404del
NM_001272042.1:c.*133_*134del	NP_001258971.1:n.*133_*134del
NM_001272043.1:c.1341-666_1341-665del	NP_001258972.1:n.1341-666_1341-665del
NM_001272044.1:c.*133_*134del	NP_001258973.1:n.*133_*134del
NM_001272060.1:c.*133_*134del	NP_001258989.1:n.*133_*134del
NM_003161.3:c.*133_*134del	NP_003152.1:n.*133_*134del
XM_011525101.1:c.*133_*134del	XP_011523403.1:n.*133_*134del
XM_011525103.1:c.*133_*134del	XP_011523405.1:n.*133_*134del
XM_011525104.1:c.*133_*134del	XP_011523406.1:n.*133_*134del
XM_011525101.3:c.*133_*134del	XP_011523403.1:n.*133_*134del
XM_011525103.3:c.*133_*134del	XP_011523405.1:n.*133_*134del
XM_017024929.1:c.*133_*134del	XP_016880418.1:n.*133_*134del
XM_017024930.2:c.*133_*134del	XP_016880419.1:n.*133_*134del
XM_017024931.2:c.*133_*134del	XP_016880420.1:n.*133_*134del
XM_017024932.2:c.*133_*134del	XP_016880421.1:n.*133_*134del
XM_017024933.2:c.*133_*134del	XP_016880422.1:n.*133_*134del
XR_001752581.2:n.1957_1958del
XR_001752582.2:n.1764_1765del
XR_001752583.2:n.1656_1657del
XR_002958051.1:n.3448_3449del
NM_003161.4:c.*133_*134del MANE Select	NP_003152.1:n.*133_*134del
NM_001272043.2:c.1341-666_1341-665del	NP_001258972.1:n.1341-666_1341-665del
NM_001369669.1:c.*133_*134del	NP_001356598.1:n.*133_*134del
NM_001369670.1:c.*133_*134del	NP_001356599.1:n.*133_*134del
NM_001369671.1:c.*133_*134del	NP_001356600.1:n.*133_*134del
NM_001369672.1:c.*133_*134del	NP_001356601.1:n.*133_*134del
NM_001369673.1:c.*1162_*1163del	NP_001356602.1:n.*1162_*1163del
NM_001369674.1:c.*1304_*1305del	NP_001356603.1:n.*1304_*1305del
NM_001369675.1:c.*1196_*1197del	NP_001356604.1:n.*1196_*1197del
NM_001369676.1:c.*1065_*1066del	NP_001356605.1:n.*1065_*1066del
NM_001369677.1:c.*1415_*1416del	NP_001356606.1:n.*1415_*1416del
NM_001369678.1:c.*1162_*1163del	NP_001356607.1:n.*1162_*1163del
NM_001369679.1:c.*1419_*1420del	NP_001356608.1:n.*1419_*1420del
NR_161455.1:n.1627_1628del
NR_161456.1:n.1778_1779del
NR_161457.1:n.1674_1675del
NR_161458.1:n.1972_1973del
NR_161459.1:n.1753_1754del
NR_161460.1:n.2018_2019del
NR_161461.1:n.1779_1780del
NR_161462.1:n.1671_1672del
NM_001272042.2:c.*133_*134del	NP_001258971.1:n.*133_*134del
NM_001272044.2:c.*133_*134del	NP_001258973.1:n.*133_*134del
NM_001272060.2:c.*133_*134del	NP_001258989.1:n.*133_*134del