Canonical Allele Identifier: CA16621294
Gene: RPS6KA3 HGNC NCBI

Linked Data

ClinVar Variation Id: 421241
ClinVar RCV Id: RCV000481699
dbSNP Id: rs1064795003
MyVariant Identifiers: chrX:g.20183040T>C (hg19) chrX:g.20164922T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.20164922T>C , CM000685.2:g.20164922T>C GRCh38
NC_000023.10:g.20183040T>C , CM000685.1:g.20183040T>C GRCh37
NC_000023.9:g.20092961T>C NCBI36
NG_007488.1:g.106711A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000379565.9:c.1741A>G MANE Select ENSP00000368884.3:p.Thr581Ala
ENST00000457145.6:c.1654A>G ENSP00000407655.2:p.Thr552Ala
ENST00000642835.1:c.1657A>G ENSP00000494769.1:p.Thr553Ala
ENST00000643073.1:c.1359A>G ENSP00000495839.1:n.1359A>G
ENST00000643085.1:c.1657A>G ENSP00000496271.1:p.Thr553Ala
ENST00000643337.1:c.1657A>G ENSP00000493487.1:p.Thr553Ala
ENST00000643402.1:c.1657A>G ENSP00000493862.1:p.Thr553Ala
ENST00000644368.1:c.1657A>G ENSP00000495776.1:p.Thr553Ala
ENST00000644893.1:c.1654A>G ENSP00000495974.1:p.Thr552Ala
ENST00000645268.1:c.*962A>G ENSP00000496226.1:n.*962A>G
ENST00000645270.1:c.1657A>G ENSP00000494967.1:p.Thr553Ala
ENST00000646610.1:c.1657A>G ENSP00000495462.1:p.Thr553Ala
ENST00000647265.1:c.1657A>G ENSP00000494220.1:p.Thr553Ala
ENST00000379565.7:c.1741A>G ENSP00000368884.3:p.Thr581Ala
ENST00000479809.1:n.408A>G
NM_004586.2:c.1741A>G NP_004577.1:p.Thr581Ala
XM_005274573.2:c.1738A>G XP_005274630.1:p.Thr580Ala
XM_005274577.2:c.1651A>G XP_005274634.1:p.Thr551Ala
XM_006724507.2:c.1654A>G XP_006724570.1:p.Thr552Ala
XM_011545555.1:c.1759A>G XP_011543857.1:p.Thr587Ala
XM_011545556.1:c.1756A>G XP_011543858.1:p.Thr586Ala
XM_011545557.1:c.1675A>G XP_011543859.1:p.Thr559Ala
XM_011545558.1:c.1675A>G XP_011543860.1:p.Thr559Ala
XM_011545559.1:c.1675A>G XP_011543861.1:p.Thr559Ala
XM_011545560.1:c.1675A>G XP_011543862.1:p.Thr559Ala
XM_011545561.1:c.1675A>G XP_011543863.1:p.Thr559Ala
XM_011545562.1:c.1672A>G XP_011543864.1:p.Thr558Ala
XM_011545563.1:c.1657A>G XP_011543865.1:p.Thr553Ala
XM_005274577.3:c.1651A>G XP_005274634.1:p.Thr551Ala
XM_006724507.3:c.1654A>G XP_006724570.1:p.Thr552Ala
XM_011545557.2:c.1675A>G XP_011543859.1:p.Thr559Ala
XM_011545558.2:c.1675A>G XP_011543860.1:p.Thr559Ala
XM_011545561.2:c.1675A>G XP_011543863.1:p.Thr559Ala
XM_011545562.2:c.1672A>G XP_011543864.1:p.Thr558Ala
XM_011545563.3:c.1657A>G XP_011543865.1:p.Thr553Ala
XM_017029713.1:c.1657A>G XP_016885202.1:p.Thr553Ala
XM_017029714.2:c.1657A>G XP_016885203.1:p.Thr553Ala
XM_017029715.2:c.1657A>G XP_016885204.1:p.Thr553Ala
XM_017029716.1:c.1657A>G XP_016885205.1:p.Thr553Ala
XM_017029717.2:c.1657A>G XP_016885206.1:p.Thr553Ala
XM_017029718.2:c.1654A>G XP_016885207.1:p.Thr552Ala
XM_017029719.2:c.1654A>G XP_016885208.1:p.Thr552Ala
NM_004586.3:c.1741A>G MANE Select NP_004577.1:p.Thr581Ala
Search 100 bp 5'
Search 100 bp 3'