Canonical Allele Identifier: CA292156511

Gene: RPS6KB1

Linked Data

• dbSNP Id: rs527419431
• gnomAD v3: 17-59946924-A-C
• gnomAD v4: 17-59946924-A-C
• MyVariant Identifiers: chr17:g.58024285A>C (hg19) ; chr17:g.59946924A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.59946924A>C , CM000679.2:g.59946924A>C	GRCh38
NC_000017.10:g.58024285A>C , CM000679.1:g.58024285A>C	GRCh37
NC_000017.9:g.55379067A>C	NCBI36
NG_029513.1:g.58843A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225577.9:c.*136A>C MANE Select	ENSP00000225577.4:n.*136A>C
ENST00000225577.8:c.*136A>C	ENSP00000225577.4:n.*136A>C
ENST00000393021.7:c.*136A>C	ENSP00000376744.3:n.*136A>C
ENST00000406116.7:c.1341-663A>C	ENSP00000384335.3:n.1341-663A>C
ENST00000443572.6:c.*136A>C	ENSP00000441993.1:n.*136A>C
ENST00000472940.5:c.*1749A>C	ENSP00000468058.1:n.*1749A>C
ENST00000475155.1:n.702A>C
ENST00000591035.1:c.149+1406A>C	ENSP00000468280.1:n.149+1406A>C
NM_001272042.1:c.*136A>C	NP_001258971.1:n.*136A>C
NM_001272043.1:c.1341-663A>C	NP_001258972.1:n.1341-663A>C
NM_001272044.1:c.*136A>C	NP_001258973.1:n.*136A>C
NM_001272060.1:c.*136A>C	NP_001258989.1:n.*136A>C
NM_003161.3:c.*136A>C	NP_003152.1:n.*136A>C
XM_011525101.1:c.*136A>C	XP_011523403.1:n.*136A>C
XM_011525103.1:c.*136A>C	XP_011523405.1:n.*136A>C
XM_011525104.1:c.*136A>C	XP_011523406.1:n.*136A>C
XM_011525101.3:c.*136A>C	XP_011523403.1:n.*136A>C
XM_011525103.3:c.*136A>C	XP_011523405.1:n.*136A>C
XM_017024929.1:c.*136A>C	XP_016880418.1:n.*136A>C
XM_017024930.2:c.*136A>C	XP_016880419.1:n.*136A>C
XM_017024931.2:c.*136A>C	XP_016880420.1:n.*136A>C
XM_017024932.2:c.*136A>C	XP_016880421.1:n.*136A>C
XM_017024933.2:c.*136A>C	XP_016880422.1:n.*136A>C
XR_001752581.2:n.1960A>C
XR_001752582.2:n.1767A>C
XR_001752583.2:n.1659A>C
XR_002958051.1:n.3451A>C
NM_003161.4:c.*136A>C MANE Select	NP_003152.1:n.*136A>C
NM_001272043.2:c.1341-663A>C	NP_001258972.1:n.1341-663A>C
NM_001369669.1:c.*136A>C	NP_001356598.1:n.*136A>C
NM_001369670.1:c.*136A>C	NP_001356599.1:n.*136A>C
NM_001369671.1:c.*136A>C	NP_001356600.1:n.*136A>C
NM_001369672.1:c.*136A>C	NP_001356601.1:n.*136A>C
NM_001369673.1:c.*1165A>C	NP_001356602.1:n.*1165A>C
NM_001369674.1:c.*1307A>C	NP_001356603.1:n.*1307A>C
NM_001369675.1:c.*1199A>C	NP_001356604.1:n.*1199A>C
NM_001369676.1:c.*1068A>C	NP_001356605.1:n.*1068A>C
NM_001369677.1:c.*1418A>C	NP_001356606.1:n.*1418A>C
NM_001369678.1:c.*1165A>C	NP_001356607.1:n.*1165A>C
NM_001369679.1:c.*1422A>C	NP_001356608.1:n.*1422A>C
NR_161455.1:n.1630A>C
NR_161456.1:n.1781A>C
NR_161457.1:n.1677A>C
NR_161458.1:n.1975A>C
NR_161459.1:n.1756A>C
NR_161460.1:n.2021A>C
NR_161461.1:n.1782A>C
NR_161462.1:n.1674A>C
NM_001272042.2:c.*136A>C	NP_001258971.1:n.*136A>C
NM_001272044.2:c.*136A>C	NP_001258973.1:n.*136A>C
NM_001272060.2:c.*136A>C	NP_001258989.1:n.*136A>C