Canonical Allele Identifier: CA2673646954

Gene: RICTOR

Linked Data

• gnomAD v4: 5-38955572-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.38955572A>G , CM000667.2:g.38955572A>G	GRCh38
NC_000005.9:g.38955674A>G , CM000667.1:g.38955674A>G	GRCh37
NC_000005.8:g.38991431A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000296782.10:c.2609+23T>C	ENSP00000296782.5:n.2609+23T>C
ENST00000503698.2:c.569+23T>C	ENSP00000518563.1:n.569+23T>C
ENST00000514735.2:c.2561+23T>C	ENSP00000423162.2:n.2561+23T>C
ENST00000711063.1:c.2609+23T>C	ENSP00000518562.1:n.2609+23T>C
ENST00000357387.8:c.2609+23T>C MANE Select	ENSP00000349959.3:n.2609+23T>C
ENST00000296782.9:c.2609+23T>C	ENSP00000296782.5:n.2609+23T>C
ENST00000357387.7:c.2609+23T>C	ENSP00000349959.3:n.2609+23T>C
ENST00000503698.1:n.569+23T>C
ENST00000511516.5:c.*1833+23T>C	ENSP00000423019.1:n.*1833+23T>C
NM_001285439.1:c.2609+23T>C	NP_001272368.1:n.2609+23T>C
NM_001285440.1:c.1754+23T>C	NP_001272369.1:n.1754+23T>C
NM_152756.4:c.2609+23T>C	NP_689969.2:n.2609+23T>C
XM_006714463.2:c.2609+23T>C	XP_006714526.1:n.2609+23T>C
XM_011514005.1:c.2609+23T>C	XP_011512307.1:n.2609+23T>C
XM_011514006.1:c.2420+23T>C	XP_011512308.1:n.2420+23T>C
XM_011514007.1:c.1754+23T>C	XP_011512309.1:n.1754+23T>C
XM_006714463.3:c.2609+23T>C	XP_006714526.1:n.2609+23T>C
XM_011514005.2:c.2609+23T>C	XP_011512307.1:n.2609+23T>C
XM_011514006.3:c.2420+23T>C	XP_011512308.1:n.2420+23T>C
XM_017009311.1:c.2561+23T>C	XP_016864800.1:n.2561+23T>C
XM_017009312.1:c.2561+23T>C	XP_016864801.1:n.2561+23T>C
XM_017009313.1:c.2450+23T>C	XP_016864802.1:n.2450+23T>C
XM_017009314.2:c.1754+23T>C	XP_016864803.1:n.1754+23T>C
XM_017009315.2:c.1754+23T>C	XP_016864804.1:n.1754+23T>C
NM_152756.5:c.2609+23T>C MANE Select	NP_689969.2:n.2609+23T>C
NM_001285439.2:c.2609+23T>C	NP_001272368.1:n.2609+23T>C
NM_001285440.2:c.1754+23T>C	NP_001272369.1:n.1754+23T>C