Canonical Allele Identifier: CA412516144

Gene: RPS6KA3

Linked Data

• MyVariant Identifiers: chrX:g.20190899T>C (hg19) ; chrX:g.20172781T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.20172781T>C , CM000685.2:g.20172781T>C	GRCh38
NC_000023.10:g.20190899T>C , CM000685.1:g.20190899T>C	GRCh37
NC_000023.9:g.20100820T>C	NCBI36
NG_007488.1:g.98852A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379565.9:c.1318A>G MANE Select	ENSP00000368884.3:p.Ile440Val
ENST00000457145.6:c.1231A>G	ENSP00000407655.2:p.Ile411Val
ENST00000642835.1:c.1234A>G	ENSP00000494769.1:p.Ile412Val
ENST00000643073.1:c.936A>G	ENSP00000495839.1:n.936A>G
ENST00000643085.1:c.1234A>G	ENSP00000496271.1:p.Ile412Val
ENST00000643337.1:c.1234A>G	ENSP00000493487.1:p.Ile412Val
ENST00000643402.1:c.1234A>G	ENSP00000493862.1:p.Ile412Val
ENST00000644368.1:c.1234A>G	ENSP00000495776.1:p.Ile412Val
ENST00000644893.1:c.1231A>G	ENSP00000495974.1:p.Ile411Val
ENST00000645268.1:c.*539A>G	ENSP00000496226.1:n.*539A>G
ENST00000645270.1:c.1234A>G	ENSP00000494967.1:p.Ile412Val
ENST00000646610.1:c.1234A>G	ENSP00000495462.1:p.Ile412Val
ENST00000647265.1:c.1234A>G	ENSP00000494220.1:p.Ile412Val
ENST00000379565.7:c.1318A>G	ENSP00000368884.3:p.Ile440Val
ENST00000479809.1:n.84A>G
NM_004586.2:c.1318A>G	NP_004577.1:p.Ile440Val
XM_005274573.2:c.1315A>G	XP_005274630.1:p.Ile439Val
XM_005274577.2:c.1228A>G	XP_005274634.1:p.Ile410Val
XM_006724507.2:c.1231A>G	XP_006724570.1:p.Ile411Val
XM_011545555.1:c.1336A>G	XP_011543857.1:p.Ile446Val
XM_011545556.1:c.1333A>G	XP_011543858.1:p.Ile445Val
XM_011545557.1:c.1252A>G	XP_011543859.1:p.Ile418Val
XM_011545558.1:c.1252A>G	XP_011543860.1:p.Ile418Val
XM_011545559.1:c.1252A>G	XP_011543861.1:p.Ile418Val
XM_011545560.1:c.1252A>G	XP_011543862.1:p.Ile418Val
XM_011545561.1:c.1252A>G	XP_011543863.1:p.Ile418Val
XM_011545562.1:c.1249A>G	XP_011543864.1:p.Ile417Val
XM_011545563.1:c.1234A>G	XP_011543865.1:p.Ile412Val
XM_005274577.3:c.1228A>G	XP_005274634.1:p.Ile410Val
XM_006724507.3:c.1231A>G	XP_006724570.1:p.Ile411Val
XM_011545557.2:c.1252A>G	XP_011543859.1:p.Ile418Val
XM_011545558.2:c.1252A>G	XP_011543860.1:p.Ile418Val
XM_011545561.2:c.1252A>G	XP_011543863.1:p.Ile418Val
XM_011545562.2:c.1249A>G	XP_011543864.1:p.Ile417Val
XM_011545563.3:c.1234A>G	XP_011543865.1:p.Ile412Val
XM_017029713.1:c.1234A>G	XP_016885202.1:p.Ile412Val
XM_017029714.2:c.1234A>G	XP_016885203.1:p.Ile412Val
XM_017029715.2:c.1234A>G	XP_016885204.1:p.Ile412Val
XM_017029716.1:c.1234A>G	XP_016885205.1:p.Ile412Val
XM_017029717.2:c.1234A>G	XP_016885206.1:p.Ile412Val
XM_017029718.2:c.1231A>G	XP_016885207.1:p.Ile411Val
XM_017029719.2:c.1231A>G	XP_016885208.1:p.Ile411Val
NM_004586.3:c.1318A>G MANE Select	NP_004577.1:p.Ile440Val