Canonical Allele Identifier: CA121631
Gene: RPS6KA3 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 11659
ClinVar RCV Id: RCV000012425
dbSNP Id: rs122454129

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.20175244G>A , CM000685.2:g.20175244G>A GRCh38
NC_000023.10:g.20193362G>A , CM000685.1:g.20193362G>A GRCh37
NC_000023.9:g.20103283G>A NCBI36
NG_007488.1:g.96389C>T

Transcript Alleles

HGVS Amino-acid change
NM_004586.2:n.1147C>T VV NP_004577.1:p.Arg383Trp
XM_005274573.2:c.1147C>T XP_005274630.1:p.Arg383Trp
XM_005274577.2:c.1060C>T XP_005274634.1:p.Arg354Trp
XM_006724507.2:c.1063C>T XP_006724570.1:p.Arg355Trp
XM_011545555.1:c.1165C>T XP_011543857.1:p.Arg389Trp
XM_011545556.1:c.1165C>T XP_011543858.1:p.Arg389Trp
XM_011545557.1:c.1081C>T XP_011543859.1:p.Arg361Trp
XM_011545558.1:c.1081C>T XP_011543860.1:p.Arg361Trp
XM_011545559.1:c.1081C>T XP_011543861.1:p.Arg361Trp
XM_011545560.1:c.1081C>T XP_011543862.1:p.Arg361Trp
XM_011545561.1:c.1081C>T XP_011543863.1:p.Arg361Trp
XM_011545562.1:c.1078C>T XP_011543864.1:p.Arg360Trp
XM_011545563.1:c.1063C>T XP_011543865.1:p.Arg355Trp
XM_005274577.3:c.1060C>T XP_005274634.1:p.Arg354Trp
XM_006724507.3:c.1063C>T XP_006724570.1:p.Arg355Trp
XM_011545557.2:c.1081C>T XP_011543859.1:p.Arg361Trp
XM_011545558.2:c.1081C>T XP_011543860.1:p.Arg361Trp
XM_011545561.2:c.1081C>T XP_011543863.1:p.Arg361Trp
XM_011545562.2:c.1078C>T XP_011543864.1:p.Arg360Trp
XM_011545563.3:c.1063C>T XP_011543865.1:p.Arg355Trp
XM_017029713.1:c.1063C>T XP_016885202.1:p.Arg355Trp
XM_017029714.2:c.1063C>T XP_016885203.1:p.Arg355Trp
XM_017029715.2:c.1063C>T XP_016885204.1:p.Arg355Trp
XM_017029716.1:c.1063C>T XP_016885205.1:p.Arg355Trp
XM_017029717.2:c.1063C>T XP_016885206.1:p.Arg355Trp
XM_017029718.2:c.1060C>T XP_016885207.1:p.Arg354Trp
XM_017029719.2:c.1063C>T XP_016885208.1:p.Arg355Trp
ENST00000379565.7:c.1147C>T ENSP00000368884.3:p.Arg383Trp