Canonical Allele Identifier: CA2487090355

Gene: MTR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236852627A= , CM000663.2:g.236852627A=	GRCh38
NC_000001.10:g.237015927A= , CM000663.1:g.237015927A=	GRCh37
NC_000001.9:g.235082550A=	NCBI36
NG_008959.1:g.62347A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.1802A= MANE Select	ENSP00000355536.5:p.His601=
ENST00000535889.6:c.1802A=	ENSP00000441845.1:p.His601=
ENST00000650888.1:c.*844A=	ENSP00000498393.1:n.*844A=
ENST00000651455.1:c.*546A=	ENSP00000498963.1:n.*546A=
ENST00000674797.2:c.1454A=	ENSP00000502299.2:p.His485=
ENST00000679569.1:n.2116A=
ENST00000679842.1:c.1802A=	ENSP00000506109.1:p.His601=
ENST00000680454.1:n.2246A=
ENST00000681102.1:c.1622A=	ENSP00000505600.1:p.His541=
ENST00000681177.1:c.1516-7206A=	ENSP00000506327.1:n.1516-7206A=
ENST00000681937.1:n.2148-7206A=
ENST00000366576.3:c.464A=	ENSP00000355535.3:p.His155=
ENST00000366577.9:c.1802A=	ENSP00000355536.5:p.His601=
ENST00000463959.1:n.1821A=
ENST00000535889.5:c.1802A=	ENSP00000441845.1:p.His601=
NM_000254.2:c.1802A=	NP_000245.2:p.His601=
NM_001291939.1:c.1802A=	NP_001278868.1:p.His601=
NM_001291940.1:c.581A=	NP_001278869.1:p.His194=
XM_005273141.3:c.1799A=	XP_005273198.1:p.His600=
XM_006711769.2:c.1802A=	XP_006711832.1:p.His601=
XM_006711770.1:c.866A=	XP_006711833.1:p.His289=
XM_011544193.1:c.1802A=	XP_011542495.1:p.His601=
XM_011544194.1:c.1970A=	XP_011542496.1:p.His657=
XM_005273141.5:c.1799A=	XP_005273198.1:p.His600=
XM_006711770.3:c.866A=	XP_006711833.1:p.His289=
XM_011544194.3:c.1970A=	XP_011542496.1:p.His657=
XM_017001329.2:c.1970A=	XP_016856818.1:p.His657=
XM_017001330.2:c.1970A=	XP_016856819.1:p.His657=
NM_001291940.2:c.581A=	NP_001278869.1:p.His194=
NM_000254.3:c.1802A= MANE Select	NP_000245.2:p.His601=