Canonical Allele Identifier: CA19799451
Gene: RPS6KA1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1002487

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26539480T>C , CM000663.2:g.26539480T>C GRCh38
NC_000001.10:g.26865971T>C , CM000663.1:g.26865971T>C GRCh37
NC_000001.9:g.26738558T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_002953.3:c.108+2511T>C VV NP_002944.2:p.=
XM_005245967.2:c.-169+2511T>C XP_005246024.1:p.=
XM_011541898.1:c.-169+2511T>C XP_011540200.1:p.=
XM_024448871.1:c.-169+2511T>C XP_024304639.1:p.=
NM_002953.4:c.108+2511T>C VV MANE Preferred NP_002944.2:p.=
ENST00000374166.8:c.108+2511T>C ENSP00000363281.4:p.=
ENST00000374168.6:c.108+2511T>C ENSP00000363283.2:p.=
ENST00000524436.5:n.254+2511T>C
ENST00000525525.5:c.*95+2511T>C ENSP00000434616.1:p.=
ENST00000526040.6:c.108+2511T>C ENSP00000436990.1:p.=
ENST00000526792.5:c.-169+2511T>C ENSP00000431651.1:p.=
ENST00000529454.5:c.-52+2511T>C ENSP00000433039.1:p.=