Canonical Allele Identifier: CA2810020299

Gene: RPS6KB1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.59946933_59946936del , CM000679.2:g.59946933_59946936del	GRCh38
NC_000017.10:g.58024294_58024297del , CM000679.1:g.58024294_58024297del	GRCh37
NC_000017.9:g.55379076_55379079del	NCBI36
NG_029513.1:g.58852_58855del

Transcript Alleles

HGVS	Amino-acid change
ENST00000225577.9:c.*145_*148del MANE Select	ENSP00000225577.4:n.*145_*148del
ENST00000225577.8:c.*145_*148del	ENSP00000225577.4:n.*145_*148del
ENST00000393021.7:c.*145_*148del	ENSP00000376744.3:n.*145_*148del
ENST00000406116.7:c.1341-654_1341-651del	ENSP00000384335.3:n.1341-654_1341-651del
ENST00000443572.6:c.*145_*148del	ENSP00000441993.1:n.*145_*148del
ENST00000472940.5:c.*1758_*1761del	ENSP00000468058.1:n.*1758_*1761del
ENST00000475155.1:n.711_714del
ENST00000591035.1:c.149+1415_149+1418del	ENSP00000468280.1:n.149+1415_149+1418del
NM_001272042.1:c.*145_*148del	NP_001258971.1:n.*145_*148del
NM_001272043.1:c.1341-654_1341-651del	NP_001258972.1:n.1341-654_1341-651del
NM_001272044.1:c.*145_*148del	NP_001258973.1:n.*145_*148del
NM_001272060.1:c.*145_*148del	NP_001258989.1:n.*145_*148del
NM_003161.3:c.*145_*148del	NP_003152.1:n.*145_*148del
XM_011525101.1:c.*145_*148del	XP_011523403.1:n.*145_*148del
XM_011525103.1:c.*145_*148del	XP_011523405.1:n.*145_*148del
XM_011525104.1:c.*145_*148del	XP_011523406.1:n.*145_*148del
XM_011525101.3:c.*145_*148del	XP_011523403.1:n.*145_*148del
XM_011525103.3:c.*145_*148del	XP_011523405.1:n.*145_*148del
XM_017024929.1:c.*145_*148del	XP_016880418.1:n.*145_*148del
XM_017024930.2:c.*145_*148del	XP_016880419.1:n.*145_*148del
XM_017024931.2:c.*145_*148del	XP_016880420.1:n.*145_*148del
XM_017024932.2:c.*145_*148del	XP_016880421.1:n.*145_*148del
XM_017024933.2:c.*145_*148del	XP_016880422.1:n.*145_*148del
XR_001752581.2:n.1969_1972del
XR_001752582.2:n.1776_1779del
XR_001752583.2:n.1668_1671del
XR_002958051.1:n.3460_3463del
NM_003161.4:c.*145_*148del MANE Select	NP_003152.1:n.*145_*148del
NM_001272043.2:c.1341-654_1341-651del	NP_001258972.1:n.1341-654_1341-651del
NM_001369669.1:c.*145_*148del	NP_001356598.1:n.*145_*148del
NM_001369670.1:c.*145_*148del	NP_001356599.1:n.*145_*148del
NM_001369671.1:c.*145_*148del	NP_001356600.1:n.*145_*148del
NM_001369672.1:c.*145_*148del	NP_001356601.1:n.*145_*148del
NM_001369673.1:c.*1174_*1177del	NP_001356602.1:n.*1174_*1177del
NM_001369674.1:c.*1316_*1319del	NP_001356603.1:n.*1316_*1319del
NM_001369675.1:c.*1208_*1211del	NP_001356604.1:n.*1208_*1211del
NM_001369676.1:c.*1077_*1080del	NP_001356605.1:n.*1077_*1080del
NM_001369677.1:c.*1427_*1430del	NP_001356606.1:n.*1427_*1430del
NM_001369678.1:c.*1174_*1177del	NP_001356607.1:n.*1174_*1177del
NM_001369679.1:c.*1431_*1434del	NP_001356608.1:n.*1431_*1434del
NR_161455.1:n.1639_1642del
NR_161456.1:n.1790_1793del
NR_161457.1:n.1686_1689del
NR_161458.1:n.1984_1987del
NR_161459.1:n.1765_1768del
NR_161460.1:n.2030_2033del
NR_161461.1:n.1791_1794del
NR_161462.1:n.1683_1686del
NM_001272042.2:c.*145_*148del	NP_001258971.1:n.*145_*148del
NM_001272044.2:c.*145_*148del	NP_001258973.1:n.*145_*148del
NM_001272060.2:c.*145_*148del	NP_001258989.1:n.*145_*148del