Canonical Allele Identifier: CA16621293
Gene: RPS6KA3 HGNC NCBI

Linked Data

ClinVar Variation Id: 422804
ClinVar RCV Id: RCV000478816
dbSNP Id: rs1064796008

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.20161642del , CM000685.2:g.20161642del GRCh38
NC_000023.10:g.20179760del , CM000685.1:g.20179760del GRCh37
NC_000023.9:g.20089681del NCBI36
NG_007488.1:g.109991del

Transcript Alleles

HGVS Amino-acid change
ENST00000379565.9:c.1959+2del MANE Select ENSP00000368884.3:n.1959+2del
ENST00000457145.6:c.1872+2del ENSP00000407655.2:n.1872+2del
ENST00000642835.1:c.1875+2del ENSP00000494769.1:n.1875+2del
ENST00000643073.1:c.1577+2del ENSP00000495839.1:n.1577+2del
ENST00000643085.1:c.1875+2del ENSP00000496271.1:n.1875+2del
ENST00000643337.1:c.1875+2del ENSP00000493487.1:n.1875+2del
ENST00000643402.1:c.1875+2del ENSP00000493862.1:n.1875+2del
ENST00000644368.1:c.1875+2del ENSP00000495776.1:n.1875+2del
ENST00000644893.1:c.1872+2del ENSP00000495974.1:n.1872+2del
ENST00000645268.1:c.*1180+2del ENSP00000496226.1:n.*1180+2del
ENST00000645270.1:c.1875+2del ENSP00000494967.1:n.1875+2del
ENST00000646610.1:c.1875+2del ENSP00000495462.1:n.1875+2del
ENST00000647265.1:c.1875+2del ENSP00000494220.1:n.1875+2del
ENST00000379565.7:c.1959+2del ENSP00000368884.3:n.1959+2del
ENST00000479809.1:n.626+2del
NM_004586.2:c.1959+2del NP_004577.1:n.1959+2del
XM_005274573.2:c.1956+2del XP_005274630.1:n.1956+2del
XM_005274577.2:c.1869+2del XP_005274634.1:n.1869+2del
XM_006724507.2:c.1872+2del XP_006724570.1:n.1872+2del
XM_011545555.1:c.1977+2del XP_011543857.1:n.1977+2del
XM_011545556.1:c.1974+2del XP_011543858.1:n.1974+2del
XM_011545557.1:c.1893+2del XP_011543859.1:n.1893+2del
XM_011545558.1:c.1893+2del XP_011543860.1:n.1893+2del
XM_011545559.1:c.1893+2del XP_011543861.1:n.1893+2del
XM_011545560.1:c.1893+2del XP_011543862.1:n.1893+2del
XM_011545561.1:c.1893+2del XP_011543863.1:n.1893+2del
XM_011545562.1:c.1890+2del XP_011543864.1:n.1890+2del
XM_011545563.1:c.1875+2del XP_011543865.1:n.1875+2del
XM_005274577.3:c.1869+2del XP_005274634.1:n.1869+2del
XM_006724507.3:c.1872+2del XP_006724570.1:n.1872+2del
XM_011545557.2:c.1893+2del XP_011543859.1:n.1893+2del
XM_011545558.2:c.1893+2del XP_011543860.1:n.1893+2del
XM_011545561.2:c.1893+2del XP_011543863.1:n.1893+2del
XM_011545562.2:c.1890+2del XP_011543864.1:n.1890+2del
XM_011545563.3:c.1875+2del XP_011543865.1:n.1875+2del
XM_017029713.1:c.1875+2del XP_016885202.1:n.1875+2del
XM_017029714.2:c.1875+2del XP_016885203.1:n.1875+2del
XM_017029715.2:c.1875+2del XP_016885204.1:n.1875+2del
XM_017029716.1:c.1875+2del XP_016885205.1:n.1875+2del
XM_017029717.2:c.1875+2del XP_016885206.1:n.1875+2del
XM_017029718.2:c.1872+2del XP_016885207.1:n.1872+2del
XM_017029719.2:c.1872+2del XP_016885208.1:n.1872+2del
NM_004586.3:c.1959+2del MANE Select NP_004577.1:n.1959+2del