Canonical Allele Identifier: CA2551001880

Gene: RPS6KA3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.20165112_20165113insGT , CM000685.2:g.20165112_20165113insGT	GRCh38
NC_000023.10:g.20183230_20183231insGT , CM000685.1:g.20183230_20183231insGT	GRCh37
NC_000023.9:g.20093151_20093152insGT	NCBI36
NG_007488.1:g.106520_106521insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379565.9:c.1603-53_1603-52insAC MANE Select	ENSP00000368884.3:n.1603-53_1603-52insAC
ENST00000457145.6:c.1516-53_1516-52insAC	ENSP00000407655.2:n.1516-53_1516-52insAC
ENST00000642835.1:c.1519-53_1519-52insAC	ENSP00000494769.1:n.1519-53_1519-52insAC
ENST00000643073.1:c.1221-53_1221-52insAC	ENSP00000495839.1:n.1221-53_1221-52insAC
ENST00000643085.1:c.1519-53_1519-52insAC	ENSP00000496271.1:n.1519-53_1519-52insAC
ENST00000643337.1:c.1519-53_1519-52insAC	ENSP00000493487.1:n.1519-53_1519-52insAC
ENST00000643402.1:c.1519-53_1519-52insAC	ENSP00000493862.1:n.1519-53_1519-52insAC
ENST00000644368.1:c.1519-53_1519-52insAC	ENSP00000495776.1:n.1519-53_1519-52insAC
ENST00000644893.1:c.1516-53_1516-52insAC	ENSP00000495974.1:n.1516-53_1516-52insAC
ENST00000645268.1:c.*824-53_*824-52insAC	ENSP00000496226.1:n.*824-53_*824-52insAC
ENST00000645270.1:c.1519-53_1519-52insAC	ENSP00000494967.1:n.1519-53_1519-52insAC
ENST00000646610.1:c.1519-53_1519-52insAC	ENSP00000495462.1:n.1519-53_1519-52insAC
ENST00000647265.1:c.1519-53_1519-52insAC	ENSP00000494220.1:n.1519-53_1519-52insAC
ENST00000379565.7:c.1603-53_1603-52insAC	ENSP00000368884.3:n.1603-53_1603-52insAC
ENST00000479809.1:n.369-152_369-151insAC
NM_004586.2:c.1603-53_1603-52insAC	NP_004577.1:n.1603-53_1603-52insAC
XM_005274573.2:c.1600-53_1600-52insAC	XP_005274630.1:n.1600-53_1600-52insAC
XM_005274577.2:c.1513-53_1513-52insAC	XP_005274634.1:n.1513-53_1513-52insAC
XM_006724507.2:c.1516-53_1516-52insAC	XP_006724570.1:n.1516-53_1516-52insAC
XM_011545555.1:c.1621-53_1621-52insAC	XP_011543857.1:n.1621-53_1621-52insAC
XM_011545556.1:c.1618-53_1618-52insAC	XP_011543858.1:n.1618-53_1618-52insAC
XM_011545557.1:c.1537-53_1537-52insAC	XP_011543859.1:n.1537-53_1537-52insAC
XM_011545558.1:c.1537-53_1537-52insAC	XP_011543860.1:n.1537-53_1537-52insAC
XM_011545559.1:c.1537-53_1537-52insAC	XP_011543861.1:n.1537-53_1537-52insAC
XM_011545560.1:c.1537-53_1537-52insAC	XP_011543862.1:n.1537-53_1537-52insAC
XM_011545561.1:c.1537-53_1537-52insAC	XP_011543863.1:n.1537-53_1537-52insAC
XM_011545562.1:c.1534-53_1534-52insAC	XP_011543864.1:n.1534-53_1534-52insAC
XM_011545563.1:c.1519-53_1519-52insAC	XP_011543865.1:n.1519-53_1519-52insAC
XM_005274577.3:c.1513-53_1513-52insAC	XP_005274634.1:n.1513-53_1513-52insAC
XM_006724507.3:c.1516-53_1516-52insAC	XP_006724570.1:n.1516-53_1516-52insAC
XM_011545557.2:c.1537-53_1537-52insAC	XP_011543859.1:n.1537-53_1537-52insAC
XM_011545558.2:c.1537-53_1537-52insAC	XP_011543860.1:n.1537-53_1537-52insAC
XM_011545561.2:c.1537-53_1537-52insAC	XP_011543863.1:n.1537-53_1537-52insAC
XM_011545562.2:c.1534-53_1534-52insAC	XP_011543864.1:n.1534-53_1534-52insAC
XM_011545563.3:c.1519-53_1519-52insAC	XP_011543865.1:n.1519-53_1519-52insAC
XM_017029713.1:c.1519-53_1519-52insAC	XP_016885202.1:n.1519-53_1519-52insAC
XM_017029714.2:c.1519-53_1519-52insAC	XP_016885203.1:n.1519-53_1519-52insAC
XM_017029715.2:c.1519-53_1519-52insAC	XP_016885204.1:n.1519-53_1519-52insAC
XM_017029716.1:c.1519-53_1519-52insAC	XP_016885205.1:n.1519-53_1519-52insAC
XM_017029717.2:c.1519-53_1519-52insAC	XP_016885206.1:n.1519-53_1519-52insAC
XM_017029718.2:c.1516-53_1516-52insAC	XP_016885207.1:n.1516-53_1516-52insAC
XM_017029719.2:c.1516-53_1516-52insAC	XP_016885208.1:n.1516-53_1516-52insAC
NM_004586.3:c.1603-53_1603-52insAC MANE Select	NP_004577.1:n.1603-53_1603-52insAC