Canonical Allele Identifier: CA2639075594
Gene: RPS6KB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.59946923A>C , CM000679.2:g.59946923A>C GRCh38
NC_000017.10:g.58024284A>C , CM000679.1:g.58024284A>C GRCh37
NC_000017.9:g.55379066A>C NCBI36
NG_029513.1:g.58842A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000225577.9:c.*135A>C MANE Select ENSP00000225577.4:n.*135A>C
ENST00000225577.8:c.*135A>C ENSP00000225577.4:n.*135A>C
ENST00000393021.7:c.*135A>C ENSP00000376744.3:n.*135A>C
ENST00000406116.7:c.1341-664A>C ENSP00000384335.3:n.1341-664A>C
ENST00000443572.6:c.*135A>C ENSP00000441993.1:n.*135A>C
ENST00000472940.5:c.*1748A>C ENSP00000468058.1:n.*1748A>C
ENST00000475155.1:n.701A>C
ENST00000591035.1:c.149+1405A>C ENSP00000468280.1:n.149+1405A>C
NM_001272042.1:c.*135A>C NP_001258971.1:n.*135A>C
NM_001272043.1:c.1341-664A>C NP_001258972.1:n.1341-664A>C
NM_001272044.1:c.*135A>C NP_001258973.1:n.*135A>C
NM_001272060.1:c.*135A>C NP_001258989.1:n.*135A>C
NM_003161.3:c.*135A>C NP_003152.1:n.*135A>C
XM_011525101.1:c.*135A>C XP_011523403.1:n.*135A>C
XM_011525103.1:c.*135A>C XP_011523405.1:n.*135A>C
XM_011525104.1:c.*135A>C XP_011523406.1:n.*135A>C
XM_011525101.3:c.*135A>C XP_011523403.1:n.*135A>C
XM_011525103.3:c.*135A>C XP_011523405.1:n.*135A>C
XM_017024929.1:c.*135A>C XP_016880418.1:n.*135A>C
XM_017024930.2:c.*135A>C XP_016880419.1:n.*135A>C
XM_017024931.2:c.*135A>C XP_016880420.1:n.*135A>C
XM_017024932.2:c.*135A>C XP_016880421.1:n.*135A>C
XM_017024933.2:c.*135A>C XP_016880422.1:n.*135A>C
XR_001752581.2:n.1959A>C
XR_001752582.2:n.1766A>C
XR_001752583.2:n.1658A>C
XR_002958051.1:n.3450A>C
NM_003161.4:c.*135A>C MANE Select NP_003152.1:n.*135A>C
NM_001272043.2:c.1341-664A>C NP_001258972.1:n.1341-664A>C
NM_001369669.1:c.*135A>C NP_001356598.1:n.*135A>C
NM_001369670.1:c.*135A>C NP_001356599.1:n.*135A>C
NM_001369671.1:c.*135A>C NP_001356600.1:n.*135A>C
NM_001369672.1:c.*135A>C NP_001356601.1:n.*135A>C
NM_001369673.1:c.*1164A>C NP_001356602.1:n.*1164A>C
NM_001369674.1:c.*1306A>C NP_001356603.1:n.*1306A>C
NM_001369675.1:c.*1198A>C NP_001356604.1:n.*1198A>C
NM_001369676.1:c.*1067A>C NP_001356605.1:n.*1067A>C
NM_001369677.1:c.*1417A>C NP_001356606.1:n.*1417A>C
NM_001369678.1:c.*1164A>C NP_001356607.1:n.*1164A>C
NM_001369679.1:c.*1421A>C NP_001356608.1:n.*1421A>C
NR_161455.1:n.1629A>C
NR_161456.1:n.1780A>C
NR_161457.1:n.1676A>C
NR_161458.1:n.1974A>C
NR_161459.1:n.1755A>C
NR_161460.1:n.2020A>C
NR_161461.1:n.1781A>C
NR_161462.1:n.1673A>C
NM_001272042.2:c.*135A>C NP_001258971.1:n.*135A>C
NM_001272044.2:c.*135A>C NP_001258973.1:n.*135A>C
NM_001272060.2:c.*135A>C NP_001258989.1:n.*135A>C