Canonical Allele Identifier: CA415913590

Gene: MTOR

Linked Data

• MyVariant Identifiers: chr1:g.11217244C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11157187C>A , CM000663.2:g.11157187C>A	GRCh38
NC_000001.10:g.11217244C>A , CM000663.1:g.11217244C>A	GRCh37
NC_000001.9:g.11139831C>A	NCBI36
NG_033239.1:g.110365G>T , LRG_734:g.110365G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000703118.1:c.4434G>T	ENSP00000515181.1:p.Leu1478=
ENST00000703131.1:n.354G>T
ENST00000703140.1:c.4221G>T	ENSP00000515197.1:p.Leu1407=
ENST00000703141.1:c.4434G>T	ENSP00000515198.1:p.Leu1478=
ENST00000703142.1:c.*1264G>T	ENSP00000515199.1:n.*1264G>T
ENST00000361445.9:c.4434G>T MANE Select	ENSP00000354558.4:p.Leu1478=
ENST00000361445.8:c.4434G>T	ENSP00000354558.4:p.Leu1478=
NM_004958.3:c.4434G>T , LRG_734t1:c.4434G>T	NP_004949.1:p.Leu1478=
XM_005263438.1:c.4434G>T	XP_005263495.1:p.Leu1478=
XM_011541166.1:c.4434G>T	XP_011539468.1:p.Leu1478=
XR_244786.1:n.4555G>T
XM_005263438.2:c.4434G>T	XP_005263495.1:p.Leu1478=
XM_011541166.2:c.4434G>T	XP_011539468.1:p.Leu1478=
XM_017000900.1:c.3753G>T	XP_016856389.1:p.Leu1251=
XM_017000901.1:c.3186G>T	XP_016856390.1:p.Leu1062=
XM_024446187.1:c.4434G>T	XP_024301955.1:p.Leu1478=
XR_001737087.1:n.4555G>T
NM_004958.4:c.4434G>T MANE Select	NP_004949.1:p.Leu1478=
NM_001386500.1:c.4434G>T	NP_001373429.1:p.Leu1478=
NM_001386501.1:c.3186G>T	NP_001373430.1:p.Leu1062=