Canonical Allele Identifier: CA255959
Gene: RPS6KA3 HGNC NCBI

Linked Data

ClinVar Variation Id: 11655
ClinVar RCV Id: RCV000012421
dbSNP Id: rs122454127
gnomAD v4: X-20195131-G-A
COSMIC: COSM295761

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.20195131G>A , CM000685.2:g.20195131G>A GRCh38
NC_000023.10:g.20213249G>A , CM000685.1:g.20213249G>A GRCh37
NC_000023.9:g.20123170G>A NCBI36
NG_007488.1:g.76502C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000379565.9:c.340C>T MANE Select ENSP00000368884.3:p.Arg114Trp
ENST00000457145.6:c.253C>T ENSP00000407655.2:p.Arg85Trp
ENST00000642835.1:c.256C>T ENSP00000494769.1:p.Arg86Trp
ENST00000643073.1:c.212-6597C>T ENSP00000495839.1:n.212-6597C>T
ENST00000643085.1:c.256C>T ENSP00000496271.1:p.Arg86Trp
ENST00000643337.1:c.256C>T ENSP00000493487.1:p.Arg86Trp
ENST00000643402.1:c.256C>T ENSP00000493862.1:p.Arg86Trp
ENST00000644368.1:c.256C>T ENSP00000495776.1:p.Arg86Trp
ENST00000644893.1:c.256C>T ENSP00000495974.1:p.Arg86Trp
ENST00000645268.1:c.139C>T ENSP00000496226.1:p.Arg47Trp
ENST00000645270.1:c.256C>T ENSP00000494967.1:p.Arg86Trp
ENST00000646610.1:c.256C>T ENSP00000495462.1:p.Arg86Trp
ENST00000647265.1:c.256C>T ENSP00000494220.1:p.Arg86Trp
ENST00000379565.7:c.340C>T ENSP00000368884.3:p.Arg114Trp
ENST00000438357.1:c.256C>T ENSP00000388512.1:p.Arg86Trp
ENST00000457145.5:c.253C>T ENSP00000407655.1:p.Arg85Trp
ENST00000492128.5:n.333C>T
NM_004586.2:c.340C>T NP_004577.1:p.Arg114Trp
XM_005274573.2:c.340C>T XP_005274630.1:p.Arg114Trp
XM_005274577.2:c.253C>T XP_005274634.1:p.Arg85Trp
XM_006724507.2:c.256C>T XP_006724570.1:p.Arg86Trp
XM_011545555.1:c.340C>T XP_011543857.1:p.Arg114Trp
XM_011545556.1:c.340C>T XP_011543858.1:p.Arg114Trp
XM_011545557.1:c.256C>T XP_011543859.1:p.Arg86Trp
XM_011545558.1:c.256C>T XP_011543860.1:p.Arg86Trp
XM_011545559.1:c.256C>T XP_011543861.1:p.Arg86Trp
XM_011545560.1:c.256C>T XP_011543862.1:p.Arg86Trp
XM_011545561.1:c.256C>T XP_011543863.1:p.Arg86Trp
XM_011545562.1:c.253C>T XP_011543864.1:p.Arg85Trp
XM_011545563.1:c.256C>T XP_011543865.1:p.Arg86Trp
XM_005274577.3:c.253C>T XP_005274634.1:p.Arg85Trp
XM_006724507.3:c.256C>T XP_006724570.1:p.Arg86Trp
XM_011545557.2:c.256C>T XP_011543859.1:p.Arg86Trp
XM_011545558.2:c.256C>T XP_011543860.1:p.Arg86Trp
XM_011545561.2:c.256C>T XP_011543863.1:p.Arg86Trp
XM_011545562.2:c.253C>T XP_011543864.1:p.Arg85Trp
XM_011545563.3:c.256C>T XP_011543865.1:p.Arg86Trp
XM_017029713.1:c.256C>T XP_016885202.1:p.Arg86Trp
XM_017029714.2:c.256C>T XP_016885203.1:p.Arg86Trp
XM_017029715.2:c.256C>T XP_016885204.1:p.Arg86Trp
XM_017029716.1:c.256C>T XP_016885205.1:p.Arg86Trp
XM_017029717.2:c.256C>T XP_016885206.1:p.Arg86Trp
XM_017029718.2:c.253C>T XP_016885207.1:p.Arg85Trp
XM_017029719.2:c.256C>T XP_016885208.1:p.Arg86Trp
NM_004586.3:c.340C>T MANE Select NP_004577.1:p.Arg114Trp