Canonical Allele Identifier: CA412512032

Gene: RPS6KA3

Linked Data

• MyVariant Identifiers: chrX:g.20173601T>G (hg19) ; chrX:g.20155483T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.20155483T>G , CM000685.2:g.20155483T>G	GRCh38
NC_000023.10:g.20173601T>G , CM000685.1:g.20173601T>G	GRCh37
NC_000023.9:g.20083522T>G	NCBI36
NG_007488.1:g.116150A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379565.9:c.2138A>C MANE Select	ENSP00000368884.3:p.Asn713Thr
ENST00000457145.6:c.2051A>C	ENSP00000407655.2:p.Asn684Thr
ENST00000642835.1:c.2054A>C	ENSP00000494769.1:p.Asn685Thr
ENST00000643073.1:c.1756A>C	ENSP00000495839.1:n.1756A>C
ENST00000643085.1:c.2054A>C	ENSP00000496271.1:p.Asn685Thr
ENST00000643337.1:c.2054A>C	ENSP00000493487.1:p.Asn685Thr
ENST00000643402.1:c.2054A>C	ENSP00000493862.1:p.Asn685Thr
ENST00000644368.1:c.2054A>C	ENSP00000495776.1:p.Asn685Thr
ENST00000644893.1:c.2051A>C	ENSP00000495974.1:p.Asn684Thr
ENST00000645268.1:c.*1359A>C	ENSP00000496226.1:n.*1359A>C
ENST00000645270.1:c.2054A>C	ENSP00000494967.1:p.Asn685Thr
ENST00000646610.1:c.2054A>C	ENSP00000495462.1:p.Asn685Thr
ENST00000647265.1:c.2054A>C	ENSP00000494220.1:p.Asn685Thr
ENST00000379565.7:c.2138A>C	ENSP00000368884.3:p.Asn713Thr
ENST00000479809.1:n.805A>C
NM_004586.2:c.2138A>C	NP_004577.1:p.Asn713Thr
XM_005274573.2:c.2135A>C	XP_005274630.1:p.Asn712Thr
XM_005274577.2:c.2048A>C	XP_005274634.1:p.Asn683Thr
XM_006724507.2:c.2051A>C	XP_006724570.1:p.Asn684Thr
XM_011545555.1:c.2156A>C	XP_011543857.1:p.Asn719Thr
XM_011545556.1:c.2153A>C	XP_011543858.1:p.Asn718Thr
XM_011545557.1:c.2072A>C	XP_011543859.1:p.Asn691Thr
XM_011545558.1:c.2072A>C	XP_011543860.1:p.Asn691Thr
XM_011545559.1:c.2072A>C	XP_011543861.1:p.Asn691Thr
XM_011545560.1:c.2072A>C	XP_011543862.1:p.Asn691Thr
XM_011545561.1:c.2072A>C	XP_011543863.1:p.Asn691Thr
XM_011545562.1:c.2069A>C	XP_011543864.1:p.Asn690Thr
XM_011545563.1:c.2054A>C	XP_011543865.1:p.Asn685Thr
XM_005274577.3:c.2048A>C	XP_005274634.1:p.Asn683Thr
XM_006724507.3:c.2051A>C	XP_006724570.1:p.Asn684Thr
XM_011545557.2:c.2072A>C	XP_011543859.1:p.Asn691Thr
XM_011545558.2:c.2072A>C	XP_011543860.1:p.Asn691Thr
XM_011545561.2:c.2072A>C	XP_011543863.1:p.Asn691Thr
XM_011545562.2:c.2069A>C	XP_011543864.1:p.Asn690Thr
XM_011545563.3:c.2054A>C	XP_011543865.1:p.Asn685Thr
XM_017029713.1:c.2054A>C	XP_016885202.1:p.Asn685Thr
XM_017029714.2:c.2054A>C	XP_016885203.1:p.Asn685Thr
XM_017029715.2:c.2054A>C	XP_016885204.1:p.Asn685Thr
XM_017029716.1:c.2054A>C	XP_016885205.1:p.Asn685Thr
XM_017029717.2:c.2054A>C	XP_016885206.1:p.Asn685Thr
XM_017029718.2:c.2051A>C	XP_016885207.1:p.Asn684Thr
XM_017029719.2:c.2051A>C	XP_016885208.1:p.Asn684Thr
NM_004586.3:c.2138A>C MANE Select	NP_004577.1:p.Asn713Thr