Canonical Allele Identifier: CA338399364

Gene: MTOR

Linked Data

• dbSNP Id: rs2100939641
• MyVariant Identifiers: chr1:g.11307877T>C (hg19) ; chr1:g.11247820T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11247820T>C , CM000663.2:g.11247820T>C	GRCh38
NC_000001.10:g.11307877T>C , CM000663.1:g.11307877T>C	GRCh37
NC_000001.9:g.11230464T>C	NCBI36
NG_033239.1:g.19732A>G , LRG_734:g.19732A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.1115A>G	ENSP00000515181.1:p.Gln372Arg
ENST00000703132.1:n.1096A>G
ENST00000703140.1:c.1115A>G	ENSP00000515197.1:p.Gln372Arg
ENST00000703141.1:c.1115A>G	ENSP00000515198.1:p.Gln372Arg
ENST00000703142.1:c.1115A>G	ENSP00000515199.1:p.Gln372Arg
ENST00000703143.1:c.1115A>G	ENSP00000515200.1:p.Gln372Arg
ENST00000703144.1:n.85A>G
ENST00000361445.9:c.1115A>G MANE Select	ENSP00000354558.4:p.Gln372Arg
ENST00000361445.8:c.1115A>G	ENSP00000354558.4:p.Gln372Arg
NM_004958.3:c.1115A>G , LRG_734t1:c.1115A>G	NP_004949.1:p.Gln372Arg
XM_005263438.1:c.1115A>G	XP_005263495.1:p.Gln372Arg
XM_011541166.1:c.1115A>G	XP_011539468.1:p.Gln372Arg
XR_244786.1:n.1236A>G
XM_005263438.2:c.1115A>G	XP_005263495.1:p.Gln372Arg
XM_011541166.2:c.1115A>G	XP_011539468.1:p.Gln372Arg
XM_017000900.1:c.434A>G	XP_016856389.1:p.Gln145Arg
XM_017000901.1:c.-25A>G	XP_016856390.1:n.-25A>G
XM_017000902.1:c.1115A>G	XP_016856391.1:p.Gln372Arg
XM_024446187.1:c.1115A>G	XP_024301955.1:p.Gln372Arg
XR_001737087.1:n.1236A>G
NM_004958.4:c.1115A>G MANE Select	NP_004949.1:p.Gln372Arg
NM_001386500.1:c.1115A>G	NP_001373429.1:p.Gln372Arg
NM_001386501.1:c.-25A>G	NP_001373430.1:n.-25A>G