Canonical Allele Identifier: CA588995

Gene: MTOR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11121400G>T , CM000663.2:g.11121400G>T	GRCh38
NC_000001.10:g.11181457G>T , CM000663.1:g.11181457G>T	GRCh37
NC_000001.9:g.11104044G>T	NCBI36
NG_033239.1:g.146152C>A , LRG_734:g.146152C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004958.4:c.6811-32C>A MANE Select	NP_004949.1:n.6811-32C>A
ENST00000361445.9:c.6811-32C>A MANE Select	ENSP00000354558.4:n.6811-32C>A
NM_001386500.1:c.6811-32C>A	NP_001373429.1:n.6811-32C>A
NM_001386501.1:c.5563-32C>A	NP_001373430.1:n.5563-32C>A
NM_004958.3:c.6811-32C>A , LRG_734t1:c.6811-32C>A	NP_004949.1:n.6811-32C>A
ENST00000361445.8:c.6811-32C>A	ENSP00000354558.4:n.6811-32C>A
ENST00000376838.5:c.1426-32C>A	ENSP00000366034.1:n.1426-32C>A
ENST00000703118.1:c.*2186-32C>A	ENSP00000515181.1:n.*2186-32C>A
ENST00000703131.1:n.2812-32C>A
ENST00000703139.1:c.1448-32C>A
ENST00000703140.1:c.6598-32C>A	ENSP00000515197.1:n.6598-32C>A
ENST00000703141.1:c.*2328-32C>A	ENSP00000515198.1:n.*2328-32C>A
ENST00000703142.1:c.*3641-32C>A	ENSP00000515199.1:n.*3641-32C>A
XM_005263438.1:c.6811-32C>A	XP_005263495.1:n.6811-32C>A
XM_005263438.2:c.6811-32C>A	XP_005263495.1:n.6811-32C>A
XM_017000900.1:c.6130-32C>A	XP_016856389.1:n.6130-32C>A
XM_017000901.1:c.5563-32C>A	XP_016856390.1:n.5563-32C>A
XM_024446187.1:c.6811-32C>A	XP_024301955.1:n.6811-32C>A
XR_001737087.1:n.6932-32C>A
XR_244786.1:n.6932-32C>A