Canonical Allele Identifier: CA415913587

Gene: MTOR

Linked Data

• ClinVar Variation Id: 1102473
• ClinVar RCV Id: RCV001425812
• dbSNP Id: rs1311967938
• gnomAD v2: 1-11217241-G-A
• MyVariant Identifiers: chr1:g.11217241G>A (hg19) ; chr1:g.11157184G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11157184G>A , CM000663.2:g.11157184G>A	GRCh38
NC_000001.10:g.11217241G>A , CM000663.1:g.11217241G>A	GRCh37
NC_000001.9:g.11139828G>A	NCBI36
NG_033239.1:g.110368C>T , LRG_734:g.110368C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000703118.1:c.4437C>T	ENSP00000515181.1:p.Gly1479=
ENST00000703131.1:n.357C>T
ENST00000703140.1:c.4224C>T	ENSP00000515197.1:p.Gly1408=
ENST00000703141.1:c.4437C>T	ENSP00000515198.1:p.Gly1479=
ENST00000703142.1:c.*1267C>T	ENSP00000515199.1:n.*1267C>T
ENST00000361445.9:c.4437C>T MANE Select	ENSP00000354558.4:p.Gly1479=
ENST00000361445.8:c.4437C>T	ENSP00000354558.4:p.Gly1479=
NM_004958.3:c.4437C>T , LRG_734t1:c.4437C>T	NP_004949.1:p.Gly1479=
XM_005263438.1:c.4437C>T	XP_005263495.1:p.Gly1479=
XM_011541166.1:c.4437C>T	XP_011539468.1:p.Gly1479=
XR_244786.1:n.4558C>T
XM_005263438.2:c.4437C>T	XP_005263495.1:p.Gly1479=
XM_011541166.2:c.4437C>T	XP_011539468.1:p.Gly1479=
XM_017000900.1:c.3756C>T	XP_016856389.1:p.Gly1252=
XM_017000901.1:c.3189C>T	XP_016856390.1:p.Gly1063=
XM_024446187.1:c.4437C>T	XP_024301955.1:p.Gly1479=
XR_001737087.1:n.4558C>T
NM_004958.4:c.4437C>T MANE Select	NP_004949.1:p.Gly1479=
NM_001386500.1:c.4437C>T	NP_001373429.1:p.Gly1479=
NM_001386501.1:c.3189C>T	NP_001373430.1:p.Gly1063=