Canonical Allele Identifier: CA359563312
Gene: RICTOR HGNC NCBI

Linked Data

dbSNP Id: rs2112890468

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.38955595C>T , CM000667.2:g.38955595C>T GRCh38
NC_000005.9:g.38955697C>T , CM000667.1:g.38955697C>T GRCh37
NC_000005.8:g.38991454C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296782.10:c.2609G>A ENSP00000296782.5:p.Arg870Lys
ENST00000503698.2:c.569G>A ENSP00000518563.1:p.Ser190Asn
ENST00000514735.2:c.2561G>A ENSP00000423162.2:p.Arg854Lys
ENST00000711063.1:c.2609G>A ENSP00000518562.1:p.Arg870Lys
ENST00000357387.8:c.2609G>A MANE Select ENSP00000349959.3:p.Arg870Lys
ENST00000296782.9:c.2609G>A ENSP00000296782.5:p.Arg870Lys
ENST00000357387.7:c.2609G>A ENSP00000349959.3:p.Arg870Lys
ENST00000503698.1:n.569G>A
ENST00000511516.5:c.*1833G>A ENSP00000423019.1:n.*1833G>A
NM_001285439.1:c.2609G>A NP_001272368.1:p.Arg870Lys
NM_001285440.1:c.1754G>A NP_001272369.1:p.Arg585Lys
NM_152756.4:c.2609G>A NP_689969.2:p.Arg870Lys
XM_006714463.2:c.2609G>A XP_006714526.1:p.Arg870Lys
XM_011514005.1:c.2609G>A XP_011512307.1:p.Arg870Lys
XM_011514006.1:c.2420G>A XP_011512308.1:p.Arg807Lys
XM_011514007.1:c.1754G>A XP_011512309.1:p.Arg585Lys
XM_006714463.3:c.2609G>A XP_006714526.1:p.Arg870Lys
XM_011514005.2:c.2609G>A XP_011512307.1:p.Arg870Lys
XM_011514006.3:c.2420G>A XP_011512308.1:p.Arg807Lys
XM_017009311.1:c.2561G>A XP_016864800.1:p.Arg854Lys
XM_017009312.1:c.2561G>A XP_016864801.1:p.Arg854Lys
XM_017009313.1:c.2450G>A XP_016864802.1:p.Arg817Lys
XM_017009314.2:c.1754G>A XP_016864803.1:p.Arg585Lys
XM_017009315.2:c.1754G>A XP_016864804.1:p.Arg585Lys
NM_152756.5:c.2609G>A MANE Select NP_689969.2:p.Arg870Lys
NM_001285439.2:c.2609G>A NP_001272368.1:p.Arg870Lys
NM_001285440.2:c.1754G>A NP_001272369.1:p.Arg585Lys