Canonical Allele Identifier: CA2810020298

Gene: RPS6KB1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.59946928T>C , CM000679.2:g.59946928T>C	GRCh38
NC_000017.10:g.58024289T>C , CM000679.1:g.58024289T>C	GRCh37
NC_000017.9:g.55379071T>C	NCBI36
NG_029513.1:g.58847T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225577.9:c.*140T>C MANE Select	ENSP00000225577.4:n.*140T>C
ENST00000225577.8:c.*140T>C	ENSP00000225577.4:n.*140T>C
ENST00000393021.7:c.*140T>C	ENSP00000376744.3:n.*140T>C
ENST00000406116.7:c.1341-659T>C	ENSP00000384335.3:n.1341-659T>C
ENST00000443572.6:c.*140T>C	ENSP00000441993.1:n.*140T>C
ENST00000472940.5:c.*1753T>C	ENSP00000468058.1:n.*1753T>C
ENST00000475155.1:n.706T>C
ENST00000591035.1:c.149+1410T>C	ENSP00000468280.1:n.149+1410T>C
NM_001272042.1:c.*140T>C	NP_001258971.1:n.*140T>C
NM_001272043.1:c.1341-659T>C	NP_001258972.1:n.1341-659T>C
NM_001272044.1:c.*140T>C	NP_001258973.1:n.*140T>C
NM_001272060.1:c.*140T>C	NP_001258989.1:n.*140T>C
NM_003161.3:c.*140T>C	NP_003152.1:n.*140T>C
XM_011525101.1:c.*140T>C	XP_011523403.1:n.*140T>C
XM_011525103.1:c.*140T>C	XP_011523405.1:n.*140T>C
XM_011525104.1:c.*140T>C	XP_011523406.1:n.*140T>C
XM_011525101.3:c.*140T>C	XP_011523403.1:n.*140T>C
XM_011525103.3:c.*140T>C	XP_011523405.1:n.*140T>C
XM_017024929.1:c.*140T>C	XP_016880418.1:n.*140T>C
XM_017024930.2:c.*140T>C	XP_016880419.1:n.*140T>C
XM_017024931.2:c.*140T>C	XP_016880420.1:n.*140T>C
XM_017024932.2:c.*140T>C	XP_016880421.1:n.*140T>C
XM_017024933.2:c.*140T>C	XP_016880422.1:n.*140T>C
XR_001752581.2:n.1964T>C
XR_001752582.2:n.1771T>C
XR_001752583.2:n.1663T>C
XR_002958051.1:n.3455T>C
NM_003161.4:c.*140T>C MANE Select	NP_003152.1:n.*140T>C
NM_001272043.2:c.1341-659T>C	NP_001258972.1:n.1341-659T>C
NM_001369669.1:c.*140T>C	NP_001356598.1:n.*140T>C
NM_001369670.1:c.*140T>C	NP_001356599.1:n.*140T>C
NM_001369671.1:c.*140T>C	NP_001356600.1:n.*140T>C
NM_001369672.1:c.*140T>C	NP_001356601.1:n.*140T>C
NM_001369673.1:c.*1169T>C	NP_001356602.1:n.*1169T>C
NM_001369674.1:c.*1311T>C	NP_001356603.1:n.*1311T>C
NM_001369675.1:c.*1203T>C	NP_001356604.1:n.*1203T>C
NM_001369676.1:c.*1072T>C	NP_001356605.1:n.*1072T>C
NM_001369677.1:c.*1422T>C	NP_001356606.1:n.*1422T>C
NM_001369678.1:c.*1169T>C	NP_001356607.1:n.*1169T>C
NM_001369679.1:c.*1426T>C	NP_001356608.1:n.*1426T>C
NR_161455.1:n.1634T>C
NR_161456.1:n.1785T>C
NR_161457.1:n.1681T>C
NR_161458.1:n.1979T>C
NR_161459.1:n.1760T>C
NR_161460.1:n.2025T>C
NR_161461.1:n.1786T>C
NR_161462.1:n.1678T>C
NM_001272042.2:c.*140T>C	NP_001258971.1:n.*140T>C
NM_001272044.2:c.*140T>C	NP_001258973.1:n.*140T>C
NM_001272060.2:c.*140T>C	NP_001258989.1:n.*140T>C