Canonical Allele Identifier: CA338372049

Gene: MTOR

Linked Data

• dbSNP Id: rs1085307114
• MyVariant Identifiers: chr1:g.11217312A>T (hg19) ; chr1:g.11157255A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11157255A>T , CM000663.2:g.11157255A>T	GRCh38
NC_000001.10:g.11217312A>T , CM000663.1:g.11217312A>T	GRCh37
NC_000001.9:g.11139899A>T	NCBI36
NG_033239.1:g.110297T>A , LRG_734:g.110297T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000703118.1:c.4366T>A	ENSP00000515181.1:p.Trp1456Arg
ENST00000703131.1:n.286T>A
ENST00000703140.1:c.4153T>A	ENSP00000515197.1:p.Trp1385Arg
ENST00000703141.1:c.4366T>A	ENSP00000515198.1:p.Trp1456Arg
ENST00000703142.1:c.*1196T>A	ENSP00000515199.1:n.*1196T>A
ENST00000361445.9:c.4366T>A MANE Select	ENSP00000354558.4:p.Trp1456Arg
ENST00000361445.8:c.4366T>A	ENSP00000354558.4:p.Trp1456Arg
NM_004958.3:c.4366T>A , LRG_734t1:c.4366T>A	NP_004949.1:p.Trp1456Arg
XM_005263438.1:c.4366T>A	XP_005263495.1:p.Trp1456Arg
XM_011541166.1:c.4366T>A	XP_011539468.1:p.Trp1456Arg
XR_244786.1:n.4487T>A
XM_005263438.2:c.4366T>A	XP_005263495.1:p.Trp1456Arg
XM_011541166.2:c.4366T>A	XP_011539468.1:p.Trp1456Arg
XM_017000900.1:c.3685T>A	XP_016856389.1:p.Trp1229Arg
XM_017000901.1:c.3118T>A	XP_016856390.1:p.Trp1040Arg
XM_024446187.1:c.4366T>A	XP_024301955.1:p.Trp1456Arg
XR_001737087.1:n.4487T>A
NM_004958.4:c.4366T>A MANE Select	NP_004949.1:p.Trp1456Arg
NM_001386500.1:c.4366T>A	NP_001373429.1:p.Trp1456Arg
NM_001386501.1:c.3118T>A	NP_001373430.1:p.Trp1040Arg