Canonical Allele Identifier: CA10898349

Gene: MTOR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11108472A>G , CM000663.2:g.11108472A>G	GRCh38
NC_000001.10:g.11168529A>G , CM000663.1:g.11168529A>G	GRCh37
NC_000001.9:g.11091116A>G	NCBI36
NG_033239.1:g.159080T>C , LRG_734:g.159080T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004958.4:c.7529-186T>C MANE Select	NP_004949.1:n.7529-186T>C
ENST00000361445.9:c.7529-186T>C MANE Select	ENSP00000354558.4:n.7529-186T>C
NM_001386500.1:c.7529-186T>C	NP_001373429.1:n.7529-186T>C
NM_001386501.1:c.6281-186T>C	NP_001373430.1:n.6281-186T>C
NM_004958.3:c.7529-186T>C , LRG_734t1:c.7529-186T>C	NP_004949.1:n.7529-186T>C
ENST00000361445.8:c.7529-186T>C	ENSP00000354558.4:n.7529-186T>C
ENST00000376838.5:c.2144-186T>C	ENSP00000366034.1:n.2144-186T>C
ENST00000473471.5:n.541-186T>C
ENST00000490931.1:n.812-186T>C
ENST00000703118.1:c.*2904-186T>C	ENSP00000515181.1:n.*2904-186T>C
ENST00000703131.1:n.3447-186T>C
ENST00000703139.1:c.2317-186T>C
ENST00000703140.1:c.7316-186T>C	ENSP00000515197.1:n.7316-186T>C
ENST00000703141.1:c.*3046-186T>C	ENSP00000515198.1:n.*3046-186T>C
ENST00000703142.1:c.*4359-186T>C	ENSP00000515199.1:n.*4359-186T>C
XM_005263438.1:c.7529-186T>C	XP_005263495.1:n.7529-186T>C
XM_005263438.2:c.7529-186T>C	XP_005263495.1:n.7529-186T>C
XM_017000900.1:c.6848-186T>C	XP_016856389.1:n.6848-186T>C
XM_017000901.1:c.6281-186T>C	XP_016856390.1:n.6281-186T>C
XM_024446187.1:c.7529-186T>C	XP_024301955.1:n.7529-186T>C
XR_001737087.1:n.7567-186T>C