Canonical Allele Identifier: CA1141581448

Gene: MTR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236897020G= , CM000663.2:g.236897020G=	GRCh38
NC_000001.10:g.237060320G= , CM000663.1:g.237060320G=	GRCh37
NC_000001.9:g.235126943G=	NCBI36
NG_008959.1:g.106740G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.3613G= MANE Select	ENSP00000355536.5:p.Glu1205=
ENST00000470570.2:n.4343G=
ENST00000535889.6:c.3460G=	ENSP00000441845.1:p.Glu1154=
ENST00000650888.1:c.*2655G=	ENSP00000498393.1:n.*2655G=
ENST00000651455.1:c.*2357G=	ENSP00000498963.1:n.*2357G=
ENST00000674797.2:c.3265G=	ENSP00000502299.2:p.Glu1089=
ENST00000679569.1:n.6740G=
ENST00000679842.1:c.3424G=	ENSP00000506109.1:p.Glu1142=
ENST00000680454.1:n.6870G=
ENST00000681102.1:c.3433G=	ENSP00000505600.1:p.Glu1145=
ENST00000681177.1:c.3175G=	ENSP00000506327.1:p.Glu1059=
ENST00000681937.1:n.3807G=
ENST00000366576.3:c.2275G=	ENSP00000355535.3:p.Glu759=
ENST00000366577.9:c.3613G=	ENSP00000355536.5:p.Glu1205=
ENST00000470570.1:n.1225G=
ENST00000535889.5:c.3460G=	ENSP00000441845.1:p.Glu1154=
NM_000254.2:c.3613G=	NP_000245.2:p.Glu1205=
NM_001291939.1:c.3460G=	NP_001278868.1:p.Glu1154=
NM_001291940.1:c.2392G=	NP_001278869.1:p.Glu798=
XM_005273141.3:c.3610G=	XP_005273198.1:p.Glu1204=
XM_006711770.1:c.2677G=	XP_006711833.1:p.Glu893=
XM_011544193.1:c.3424G=	XP_011542495.1:p.Glu1142=
XM_011544194.1:c.3781G=	XP_011542496.1:p.Glu1261=
XM_005273141.5:c.3610G=	XP_005273198.1:p.Glu1204=
XM_006711770.3:c.2677G=	XP_006711833.1:p.Glu893=
XM_011544194.3:c.3781G=	XP_011542496.1:p.Glu1261=
XM_017001329.2:c.3628G=	XP_016856818.1:p.Glu1210=
XM_017001330.2:c.3592G=	XP_016856819.1:p.Glu1198=
NM_001291940.2:c.2392G=	NP_001278869.1:p.Glu798=
NM_000254.3:c.3613G= MANE Select	NP_000245.2:p.Glu1205=