Canonical Allele Identifier: CA640848019

Gene: RPS6KA3

Linked Data

• dbSNP Id: rs1250749344
• gnomAD v2: X-20173500-T-C
• gnomAD v3: X-20155382-T-C
• gnomAD v4: X-20155382-T-C
• MyVariant Identifiers: chrX:g.20173500T>C (hg19) ; chrX:g.20155382T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.20155382T>C , CM000685.2:g.20155382T>C	GRCh38
NC_000023.10:g.20173500T>C , CM000685.1:g.20173500T>C	GRCh37
NC_000023.9:g.20083421T>C	NCBI36
NG_007488.1:g.116251A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000379565.9:c.*16A>G MANE Select	ENSP00000368884.3:n.*16A>G
ENST00000457145.6:c.*16A>G	ENSP00000407655.2:n.*16A>G
ENST00000642835.1:c.*16A>G	ENSP00000494769.1:n.*16A>G
ENST00000643073.1:c.1857A>G	ENSP00000495839.1:n.1857A>G
ENST00000643085.1:c.*16A>G	ENSP00000496271.1:n.*16A>G
ENST00000643337.1:c.*16A>G	ENSP00000493487.1:n.*16A>G
ENST00000643402.1:c.*16A>G	ENSP00000493862.1:n.*16A>G
ENST00000644368.1:c.*16A>G	ENSP00000495776.1:n.*16A>G
ENST00000644893.1:c.*16A>G	ENSP00000495974.1:n.*16A>G
ENST00000645268.1:c.*1460A>G	ENSP00000496226.1:n.*1460A>G
ENST00000645270.1:c.*16A>G	ENSP00000494967.1:n.*16A>G
ENST00000646610.1:c.*16A>G	ENSP00000495462.1:n.*16A>G
ENST00000647265.1:c.*16A>G	ENSP00000494220.1:n.*16A>G
ENST00000379565.7:c.*16A>G	ENSP00000368884.3:n.*16A>G
NM_004586.2:c.2239A>G	NP_004577.1:n.2239A>G
XM_005274573.2:c.*16A>G	XP_005274630.1:n.*16A>G
XM_005274577.2:c.*16A>G	XP_005274634.1:n.*16A>G
XM_006724507.2:c.*16A>G	XP_006724570.1:n.*16A>G
XM_011545555.1:c.2209+48A>G	XP_011543857.1:n.2209+48A>G
XM_011545556.1:c.*16A>G	XP_011543858.1:n.*16A>G
XM_011545557.1:c.*16A>G	XP_011543859.1:n.*16A>G
XM_011545558.1:c.*16A>G	XP_011543860.1:n.*16A>G
XM_011545559.1:c.*16A>G	XP_011543861.1:n.*16A>G
XM_011545560.1:c.*16A>G	XP_011543862.1:n.*16A>G
XM_011545561.1:c.*16A>G	XP_011543863.1:n.*16A>G
XM_011545562.1:c.*16A>G	XP_011543864.1:n.*16A>G
XM_011545563.1:c.*16A>G	XP_011543865.1:n.*16A>G
XM_005274577.3:c.*16A>G	XP_005274634.1:n.*16A>G
XM_006724507.3:c.*16A>G	XP_006724570.1:n.*16A>G
XM_011545557.2:c.*16A>G	XP_011543859.1:n.*16A>G
XM_011545558.2:c.*16A>G	XP_011543860.1:n.*16A>G
XM_011545561.2:c.*16A>G	XP_011543863.1:n.*16A>G
XM_011545562.2:c.*16A>G	XP_011543864.1:n.*16A>G
XM_011545563.3:c.*16A>G	XP_011543865.1:n.*16A>G
XM_017029713.1:c.*16A>G	XP_016885202.1:n.*16A>G
XM_017029714.2:c.*16A>G	XP_016885203.1:n.*16A>G
XM_017029715.2:c.*16A>G	XP_016885204.1:n.*16A>G
XM_017029716.1:c.*16A>G	XP_016885205.1:n.*16A>G
XM_017029717.2:c.*16A>G	XP_016885206.1:n.*16A>G
XM_017029718.2:c.*16A>G	XP_016885207.1:n.*16A>G
XM_017029719.2:c.*16A>G	XP_016885208.1:n.*16A>G
NM_004586.3:c.*16A>G MANE Select	NP_004577.1:n.*16A>G