Canonical Allele Identifier: CA415913571

Gene: MTOR

Linked Data

• MyVariant Identifiers: chr1:g.11217232G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11157175G>T , CM000663.2:g.11157175G>T	GRCh38
NC_000001.10:g.11217232G>T , CM000663.1:g.11217232G>T	GRCh37
NC_000001.9:g.11139819G>T	NCBI36
NG_033239.1:g.110377C>A , LRG_734:g.110377C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000703118.1:c.4446C>A	ENSP00000515181.1:p.Arg1482=
ENST00000703131.1:n.366C>A
ENST00000703140.1:c.4233C>A	ENSP00000515197.1:p.Arg1411=
ENST00000703141.1:c.4446C>A	ENSP00000515198.1:p.Arg1482=
ENST00000703142.1:c.*1276C>A	ENSP00000515199.1:n.*1276C>A
ENST00000361445.9:c.4446C>A MANE Select	ENSP00000354558.4:p.Arg1482=
ENST00000361445.8:c.4446C>A	ENSP00000354558.4:p.Arg1482=
NM_004958.3:c.4446C>A , LRG_734t1:c.4446C>A	NP_004949.1:p.Arg1482=
XM_005263438.1:c.4446C>A	XP_005263495.1:p.Arg1482=
XM_011541166.1:c.4446C>A	XP_011539468.1:p.Arg1482=
XR_244786.1:n.4567C>A
XM_005263438.2:c.4446C>A	XP_005263495.1:p.Arg1482=
XM_011541166.2:c.4446C>A	XP_011539468.1:p.Arg1482=
XM_017000900.1:c.3765C>A	XP_016856389.1:p.Arg1255=
XM_017000901.1:c.3198C>A	XP_016856390.1:p.Arg1066=
XM_024446187.1:c.4446C>A	XP_024301955.1:p.Arg1482=
XR_001737087.1:n.4567C>A
NM_004958.4:c.4446C>A MANE Select	NP_004949.1:p.Arg1482=
NM_001386500.1:c.4446C>A	NP_001373429.1:p.Arg1482=
NM_001386501.1:c.3198C>A	NP_001373430.1:p.Arg1066=