Canonical Allele Identifier: CA359569650

Gene: RICTOR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.38964867T>C , CM000667.2:g.38964867T>C	GRCh38
NC_000005.9:g.38964969T>C , CM000667.1:g.38964969T>C	GRCh37
NC_000005.8:g.39000726T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_152756.5:c.1325A>G MANE Select	NP_689969.2:p.His442Arg
ENST00000357387.8:c.1325A>G MANE Select	ENSP00000349959.3:p.His442Arg
NM_001285439.1:c.1325A>G	NP_001272368.1:p.His442Arg
NM_001285439.2:c.1325A>G	NP_001272368.1:p.His442Arg
NM_001285440.1:c.470A>G	NP_001272369.1:p.His157Arg
NM_001285440.2:c.470A>G	NP_001272369.1:p.His157Arg
NM_152756.4:c.1325A>G	NP_689969.2:p.His442Arg
ENST00000296782.10:c.1325A>G	ENSP00000296782.5:p.His442Arg
ENST00000296782.9:c.1325A>G	ENSP00000296782.5:p.His442Arg
ENST00000357387.7:c.1325A>G	ENSP00000349959.3:p.His442Arg
ENST00000509567.5:n.472A>G
ENST00000511516.5:c.*549A>G	ENSP00000423019.1:n.*549A>G
ENST00000514735.2:c.1277A>G	ENSP00000423162.2:p.His426Arg
ENST00000711063.1:c.1325A>G	ENSP00000518562.1:p.His442Arg
XM_006714463.2:c.1325A>G	XP_006714526.1:p.His442Arg
XM_006714463.3:c.1325A>G	XP_006714526.1:p.His442Arg
XM_011514005.1:c.1325A>G	XP_011512307.1:p.His442Arg
XM_011514005.2:c.1325A>G	XP_011512307.1:p.His442Arg
XM_011514006.1:c.1136A>G	XP_011512308.1:p.His379Arg
XM_011514006.3:c.1136A>G	XP_011512308.1:p.His379Arg
XM_011514007.1:c.470A>G	XP_011512309.1:p.His157Arg
XM_017009311.1:c.1277A>G	XP_016864800.1:p.His426Arg
XM_017009312.1:c.1277A>G	XP_016864801.1:p.His426Arg
XM_017009313.1:c.1166A>G	XP_016864802.1:p.His389Arg
XM_017009314.2:c.470A>G	XP_016864803.1:p.His157Arg
XM_017009315.2:c.470A>G	XP_016864804.1:p.His157Arg