Canonical Allele Identifier: CA1540476108

Gene: RICTOR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.38955681G= , CM000667.2:g.38955681G=	GRCh38
NC_000005.9:g.38955783G= , CM000667.1:g.38955783G=	GRCh37
NC_000005.8:g.38991540G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296782.10:c.2523C=	ENSP00000296782.5:p.Asp841=
ENST00000503698.2:c.483C=	ENSP00000518563.1:p.Asp161=
ENST00000514735.2:c.2475C=	ENSP00000423162.2:p.Asp825=
ENST00000711063.1:c.2523C=	ENSP00000518562.1:p.Asp841=
ENST00000357387.8:c.2523C= MANE Select	ENSP00000349959.3:p.Asp841=
ENST00000296782.9:c.2523C=	ENSP00000296782.5:p.Asp841=
ENST00000357387.7:c.2523C=	ENSP00000349959.3:p.Asp841=
ENST00000503698.1:n.483C=
ENST00000511516.5:c.*1747C=	ENSP00000423019.1:n.*1747C=
NM_001285439.1:c.2523C=	NP_001272368.1:p.Asp841=
NM_001285440.1:c.1668C=	NP_001272369.1:p.Asp556=
NM_152756.4:c.2523C=	NP_689969.2:p.Asp841=
XM_006714463.2:c.2523C=	XP_006714526.1:p.Asp841=
XM_011514005.1:c.2523C=	XP_011512307.1:p.Asp841=
XM_011514006.1:c.2334C=	XP_011512308.1:p.Asp778=
XM_011514007.1:c.1668C=	XP_011512309.1:p.Asp556=
XM_006714463.3:c.2523C=	XP_006714526.1:p.Asp841=
XM_011514005.2:c.2523C=	XP_011512307.1:p.Asp841=
XM_011514006.3:c.2334C=	XP_011512308.1:p.Asp778=
XM_017009311.1:c.2475C=	XP_016864800.1:p.Asp825=
XM_017009312.1:c.2475C=	XP_016864801.1:p.Asp825=
XM_017009313.1:c.2364C=	XP_016864802.1:p.Asp788=
XM_017009314.2:c.1668C=	XP_016864803.1:p.Asp556=
XM_017009315.2:c.1668C=	XP_016864804.1:p.Asp556=
NM_152756.5:c.2523C= MANE Select	NP_689969.2:p.Asp841=
NM_001285439.2:c.2523C=	NP_001272368.1:p.Asp841=
NM_001285440.2:c.1668C=	NP_001272369.1:p.Asp556=