Canonical Allele Identifier: CA2693275806

Gene: RPS6KA3

Linked Data

• gnomAD v4: X-20155547-CAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.20155550_20155551del , CM000685.2:g.20155550_20155551del	GRCh38
NC_000023.10:g.20173668_20173669del , CM000685.1:g.20173668_20173669del	GRCh37
NC_000023.9:g.20083589_20083590del	NCBI36
NG_007488.1:g.116084_116085del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379565.9:c.2101-29_2101-28del MANE Select	ENSP00000368884.3:n.2101-29_2101-28del
ENST00000457145.6:c.2014-29_2014-28del	ENSP00000407655.2:n.2014-29_2014-28del
ENST00000642835.1:c.2017-29_2017-28del	ENSP00000494769.1:n.2017-29_2017-28del
ENST00000643073.1:c.1719-29_1719-28del	ENSP00000495839.1:n.1719-29_1719-28del
ENST00000643085.1:c.2017-29_2017-28del	ENSP00000496271.1:n.2017-29_2017-28del
ENST00000643337.1:c.2017-29_2017-28del	ENSP00000493487.1:n.2017-29_2017-28del
ENST00000643402.1:c.2017-29_2017-28del	ENSP00000493862.1:n.2017-29_2017-28del
ENST00000644368.1:c.2017-29_2017-28del	ENSP00000495776.1:n.2017-29_2017-28del
ENST00000644893.1:c.2014-29_2014-28del	ENSP00000495974.1:n.2014-29_2014-28del
ENST00000645268.1:c.*1322-29_*1322-28del	ENSP00000496226.1:n.*1322-29_*1322-28del
ENST00000645270.1:c.2017-29_2017-28del	ENSP00000494967.1:n.2017-29_2017-28del
ENST00000646610.1:c.2017-29_2017-28del	ENSP00000495462.1:n.2017-29_2017-28del
ENST00000647265.1:c.2017-29_2017-28del	ENSP00000494220.1:n.2017-29_2017-28del
ENST00000379565.7:c.2101-29_2101-28del	ENSP00000368884.3:n.2101-29_2101-28del
ENST00000479809.1:n.768-29_768-28del
NM_004586.2:c.2101-29_2101-28del	NP_004577.1:n.2101-29_2101-28del
XM_005274573.2:c.2098-29_2098-28del	XP_005274630.1:n.2098-29_2098-28del
XM_005274577.2:c.2011-29_2011-28del	XP_005274634.1:n.2011-29_2011-28del
XM_006724507.2:c.2014-29_2014-28del	XP_006724570.1:n.2014-29_2014-28del
XM_011545555.1:c.2119-29_2119-28del	XP_011543857.1:n.2119-29_2119-28del
XM_011545556.1:c.2116-29_2116-28del	XP_011543858.1:n.2116-29_2116-28del
XM_011545557.1:c.2035-29_2035-28del	XP_011543859.1:n.2035-29_2035-28del
XM_011545558.1:c.2035-29_2035-28del	XP_011543860.1:n.2035-29_2035-28del
XM_011545559.1:c.2035-29_2035-28del	XP_011543861.1:n.2035-29_2035-28del
XM_011545560.1:c.2035-29_2035-28del	XP_011543862.1:n.2035-29_2035-28del
XM_011545561.1:c.2035-29_2035-28del	XP_011543863.1:n.2035-29_2035-28del
XM_011545562.1:c.2032-29_2032-28del	XP_011543864.1:n.2032-29_2032-28del
XM_011545563.1:c.2017-29_2017-28del	XP_011543865.1:n.2017-29_2017-28del
XM_005274577.3:c.2011-29_2011-28del	XP_005274634.1:n.2011-29_2011-28del
XM_006724507.3:c.2014-29_2014-28del	XP_006724570.1:n.2014-29_2014-28del
XM_011545557.2:c.2035-29_2035-28del	XP_011543859.1:n.2035-29_2035-28del
XM_011545558.2:c.2035-29_2035-28del	XP_011543860.1:n.2035-29_2035-28del
XM_011545561.2:c.2035-29_2035-28del	XP_011543863.1:n.2035-29_2035-28del
XM_011545562.2:c.2032-29_2032-28del	XP_011543864.1:n.2032-29_2032-28del
XM_011545563.3:c.2017-29_2017-28del	XP_011543865.1:n.2017-29_2017-28del
XM_017029713.1:c.2017-29_2017-28del	XP_016885202.1:n.2017-29_2017-28del
XM_017029714.2:c.2017-29_2017-28del	XP_016885203.1:n.2017-29_2017-28del
XM_017029715.2:c.2017-29_2017-28del	XP_016885204.1:n.2017-29_2017-28del
XM_017029716.1:c.2017-29_2017-28del	XP_016885205.1:n.2017-29_2017-28del
XM_017029717.2:c.2017-29_2017-28del	XP_016885206.1:n.2017-29_2017-28del
XM_017029718.2:c.2014-29_2014-28del	XP_016885207.1:n.2014-29_2014-28del
XM_017029719.2:c.2014-29_2014-28del	XP_016885208.1:n.2014-29_2014-28del
NM_004586.3:c.2101-29_2101-28del MANE Select	NP_004577.1:n.2101-29_2101-28del