Canonical Allele Identifier: CA338371628

Gene: MTOR

Linked Data

• dbSNP Id: rs2100567274
• MyVariant Identifiers: chr1:g.11217243C>T (hg19) ; chr1:g.11157186C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11157186C>T , CM000663.2:g.11157186C>T	GRCh38
NC_000001.10:g.11217243C>T , CM000663.1:g.11217243C>T	GRCh37
NC_000001.9:g.11139830C>T	NCBI36
NG_033239.1:g.110366G>A , LRG_734:g.110366G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.4435G>A	ENSP00000515181.1:p.Gly1479Ser
ENST00000703131.1:n.355G>A
ENST00000703140.1:c.4222G>A	ENSP00000515197.1:p.Gly1408Ser
ENST00000703141.1:c.4435G>A	ENSP00000515198.1:p.Gly1479Ser
ENST00000703142.1:c.*1265G>A	ENSP00000515199.1:n.*1265G>A
ENST00000361445.9:c.4435G>A MANE Select	ENSP00000354558.4:p.Gly1479Ser
ENST00000361445.8:c.4435G>A	ENSP00000354558.4:p.Gly1479Ser
NM_004958.3:c.4435G>A , LRG_734t1:c.4435G>A	NP_004949.1:p.Gly1479Ser
XM_005263438.1:c.4435G>A	XP_005263495.1:p.Gly1479Ser
XM_011541166.1:c.4435G>A	XP_011539468.1:p.Gly1479Ser
XR_244786.1:n.4556G>A
XM_005263438.2:c.4435G>A	XP_005263495.1:p.Gly1479Ser
XM_011541166.2:c.4435G>A	XP_011539468.1:p.Gly1479Ser
XM_017000900.1:c.3754G>A	XP_016856389.1:p.Gly1252Ser
XM_017000901.1:c.3187G>A	XP_016856390.1:p.Gly1063Ser
XM_024446187.1:c.4435G>A	XP_024301955.1:p.Gly1479Ser
XR_001737087.1:n.4556G>A
NM_004958.4:c.4435G>A MANE Select	NP_004949.1:p.Gly1479Ser
NM_001386500.1:c.4435G>A	NP_001373429.1:p.Gly1479Ser
NM_001386501.1:c.3187G>A	NP_001373430.1:p.Gly1063Ser