Canonical Allele Identifier: CA443950925

Gene: RICTOR

Linked Data

• MyVariant Identifiers: chr5:g.38955698T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.38955596T>G , CM000667.2:g.38955596T>G	GRCh38
NC_000005.9:g.38955698T>G , CM000667.1:g.38955698T>G	GRCh37
NC_000005.8:g.38991455T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296782.10:c.2608A>C	ENSP00000296782.5:p.Arg870=
ENST00000503698.2:c.568A>C	ENSP00000518563.1:p.Ser190Arg
ENST00000514735.2:c.2560A>C	ENSP00000423162.2:p.Arg854=
ENST00000711063.1:c.2608A>C	ENSP00000518562.1:p.Arg870=
ENST00000357387.8:c.2608A>C MANE Select	ENSP00000349959.3:p.Arg870=
ENST00000296782.9:c.2608A>C	ENSP00000296782.5:p.Arg870=
ENST00000357387.7:c.2608A>C	ENSP00000349959.3:p.Arg870=
ENST00000503698.1:n.568A>C
ENST00000511516.5:c.*1832A>C	ENSP00000423019.1:n.*1832A>C
NM_001285439.1:c.2608A>C	NP_001272368.1:p.Arg870=
NM_001285440.1:c.1753A>C	NP_001272369.1:p.Arg585=
NM_152756.4:c.2608A>C	NP_689969.2:p.Arg870=
XM_006714463.2:c.2608A>C	XP_006714526.1:p.Arg870=
XM_011514005.1:c.2608A>C	XP_011512307.1:p.Arg870=
XM_011514006.1:c.2419A>C	XP_011512308.1:p.Arg807=
XM_011514007.1:c.1753A>C	XP_011512309.1:p.Arg585=
XM_006714463.3:c.2608A>C	XP_006714526.1:p.Arg870=
XM_011514005.2:c.2608A>C	XP_011512307.1:p.Arg870=
XM_011514006.3:c.2419A>C	XP_011512308.1:p.Arg807=
XM_017009311.1:c.2560A>C	XP_016864800.1:p.Arg854=
XM_017009312.1:c.2560A>C	XP_016864801.1:p.Arg854=
XM_017009313.1:c.2449A>C	XP_016864802.1:p.Arg817=
XM_017009314.2:c.1753A>C	XP_016864803.1:p.Arg585=
XM_017009315.2:c.1753A>C	XP_016864804.1:p.Arg585=
NM_152756.5:c.2608A>C MANE Select	NP_689969.2:p.Arg870=
NM_001285439.2:c.2608A>C	NP_001272368.1:p.Arg870=
NM_001285440.2:c.1753A>C	NP_001272369.1:p.Arg585=