Canonical Allele Identifier: CA412514339

Gene: RPS6KA3

Linked Data

• MyVariant Identifiers: chrX:g.20183168C>A (hg19) ; chrX:g.20165050C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.20165050C>A , CM000685.2:g.20165050C>A	GRCh38
NC_000023.10:g.20183168C>A , CM000685.1:g.20183168C>A	GRCh37
NC_000023.9:g.20093089C>A	NCBI36
NG_007488.1:g.106583G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379565.9:c.1613G>T MANE Select	ENSP00000368884.3:p.Arg538Ile
ENST00000457145.6:c.1526G>T	ENSP00000407655.2:p.Arg509Ile
ENST00000642835.1:c.1529G>T	ENSP00000494769.1:p.Arg510Ile
ENST00000643073.1:c.1231G>T	ENSP00000495839.1:n.1231G>T
ENST00000643085.1:c.1529G>T	ENSP00000496271.1:p.Arg510Ile
ENST00000643337.1:c.1529G>T	ENSP00000493487.1:p.Arg510Ile
ENST00000643402.1:c.1529G>T	ENSP00000493862.1:p.Arg510Ile
ENST00000644368.1:c.1529G>T	ENSP00000495776.1:p.Arg510Ile
ENST00000644893.1:c.1526G>T	ENSP00000495974.1:p.Arg509Ile
ENST00000645268.1:c.*834G>T	ENSP00000496226.1:n.*834G>T
ENST00000645270.1:c.1529G>T	ENSP00000494967.1:p.Arg510Ile
ENST00000646610.1:c.1529G>T	ENSP00000495462.1:p.Arg510Ile
ENST00000647265.1:c.1529G>T	ENSP00000494220.1:p.Arg510Ile
ENST00000379565.7:c.1613G>T	ENSP00000368884.3:p.Arg538Ile
ENST00000479809.1:n.369-89G>T
NM_004586.2:c.1613G>T	NP_004577.1:p.Arg538Ile
XM_005274573.2:c.1610G>T	XP_005274630.1:p.Arg537Ile
XM_005274577.2:c.1523G>T	XP_005274634.1:p.Arg508Ile
XM_006724507.2:c.1526G>T	XP_006724570.1:p.Arg509Ile
XM_011545555.1:c.1631G>T	XP_011543857.1:p.Arg544Ile
XM_011545556.1:c.1628G>T	XP_011543858.1:p.Arg543Ile
XM_011545557.1:c.1547G>T	XP_011543859.1:p.Arg516Ile
XM_011545558.1:c.1547G>T	XP_011543860.1:p.Arg516Ile
XM_011545559.1:c.1547G>T	XP_011543861.1:p.Arg516Ile
XM_011545560.1:c.1547G>T	XP_011543862.1:p.Arg516Ile
XM_011545561.1:c.1547G>T	XP_011543863.1:p.Arg516Ile
XM_011545562.1:c.1544G>T	XP_011543864.1:p.Arg515Ile
XM_011545563.1:c.1529G>T	XP_011543865.1:p.Arg510Ile
XM_005274577.3:c.1523G>T	XP_005274634.1:p.Arg508Ile
XM_006724507.3:c.1526G>T	XP_006724570.1:p.Arg509Ile
XM_011545557.2:c.1547G>T	XP_011543859.1:p.Arg516Ile
XM_011545558.2:c.1547G>T	XP_011543860.1:p.Arg516Ile
XM_011545561.2:c.1547G>T	XP_011543863.1:p.Arg516Ile
XM_011545562.2:c.1544G>T	XP_011543864.1:p.Arg515Ile
XM_011545563.3:c.1529G>T	XP_011543865.1:p.Arg510Ile
XM_017029713.1:c.1529G>T	XP_016885202.1:p.Arg510Ile
XM_017029714.2:c.1529G>T	XP_016885203.1:p.Arg510Ile
XM_017029715.2:c.1529G>T	XP_016885204.1:p.Arg510Ile
XM_017029716.1:c.1529G>T	XP_016885205.1:p.Arg510Ile
XM_017029717.2:c.1529G>T	XP_016885206.1:p.Arg510Ile
XM_017029718.2:c.1526G>T	XP_016885207.1:p.Arg509Ile
XM_017029719.2:c.1526G>T	XP_016885208.1:p.Arg509Ile
NM_004586.3:c.1613G>T MANE Select	NP_004577.1:p.Arg538Ile