Canonical Allele Identifier: CA17937495

Gene: MTOR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11124290A>G , CM000663.2:g.11124290A>G	GRCh38
NC_000001.10:g.11184347A>G , CM000663.1:g.11184347A>G	GRCh37
NC_000001.9:g.11106934A>G	NCBI36
NG_033239.1:g.143262T>C , LRG_734:g.143262T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004958.4:c.6662+208T>C MANE Select	NP_004949.1:n.6662+208T>C
ENST00000361445.9:c.6662+208T>C MANE Select	ENSP00000354558.4:n.6662+208T>C
NM_001386500.1:c.6662+208T>C	NP_001373429.1:n.6662+208T>C
NM_001386501.1:c.5414+208T>C	NP_001373430.1:n.5414+208T>C
NM_004958.3:c.6662+208T>C , LRG_734t1:c.6662+208T>C	NP_004949.1:n.6662+208T>C
ENST00000361445.8:c.6662+208T>C	ENSP00000354558.4:n.6662+208T>C
ENST00000376838.5:c.1277+208T>C	ENSP00000366034.1:n.1277+208T>C
ENST00000703118.1:c.*2037+208T>C	ENSP00000515181.1:n.*2037+208T>C
ENST00000703131.1:n.2663+208T>C
ENST00000703139.1:c.1299+208T>C
ENST00000703140.1:c.6449+208T>C	ENSP00000515197.1:n.6449+208T>C
ENST00000703141.1:c.*2179+208T>C	ENSP00000515198.1:n.*2179+208T>C
ENST00000703142.1:c.*3492+208T>C	ENSP00000515199.1:n.*3492+208T>C
XM_005263438.1:c.6662+208T>C	XP_005263495.1:n.6662+208T>C
XM_005263438.2:c.6662+208T>C	XP_005263495.1:n.6662+208T>C
XM_017000900.1:c.5981+208T>C	XP_016856389.1:n.5981+208T>C
XM_017000901.1:c.5414+208T>C	XP_016856390.1:n.5414+208T>C
XM_024446187.1:c.6662+208T>C	XP_024301955.1:n.6662+208T>C
XR_001737087.1:n.6783+208T>C
XR_244786.1:n.6783+208T>C