Canonical Allele Identifier: CA2487080869

Gene: MTR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236829215G= , CM000663.2:g.236829215G=	GRCh38
NC_000001.10:g.236992515G= , CM000663.1:g.236992515G=	GRCh37
NC_000001.9:g.235059138G=	NCBI36
NG_008959.1:g.38935G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.1022G= MANE Select	ENSP00000355536.5:p.Cys341=
ENST00000535889.6:c.1022G=	ENSP00000441845.1:p.Cys341=
ENST00000650888.1:c.*64G=	ENSP00000498393.1:n.*64G=
ENST00000651455.1:c.1022G=	ENSP00000498963.1:p.Cys341=
ENST00000674797.2:c.674G=	ENSP00000502299.2:p.Cys225=
ENST00000679569.1:n.1336G=
ENST00000679842.1:c.1022G=	ENSP00000506109.1:p.Cys341=
ENST00000680454.1:n.1466G=
ENST00000681102.1:c.1022G=	ENSP00000505600.1:p.Cys341=
ENST00000681177.1:c.1022G=	ENSP00000506327.1:p.Cys341=
ENST00000681937.1:n.1654G=
ENST00000366577.9:c.1022G=	ENSP00000355536.5:p.Cys341=
ENST00000463959.1:n.1041G=
ENST00000535889.5:c.1022G=	ENSP00000441845.1:p.Cys341=
NM_000254.2:c.1022G=	NP_000245.2:p.Cys341=
NM_001291939.1:c.1022G=	NP_001278868.1:p.Cys341=
NM_001291940.1:c.-87G=	NP_001278869.1:n.-87G=
XM_005273141.3:c.1019G=	XP_005273198.1:p.Cys340=
XM_006711769.2:c.1022G=	XP_006711832.1:p.Cys341=
XM_006711770.1:c.86G=	XP_006711833.1:p.Cys29=
XM_011544193.1:c.1022G=	XP_011542495.1:p.Cys341=
XM_011544194.1:c.1190G=	XP_011542496.1:p.Cys397=
XM_005273141.5:c.1019G=	XP_005273198.1:p.Cys340=
XM_006711770.3:c.86G=	XP_006711833.1:p.Cys29=
XM_011544194.3:c.1190G=	XP_011542496.1:p.Cys397=
XM_017001329.2:c.1190G=	XP_016856818.1:p.Cys397=
XM_017001330.2:c.1190G=	XP_016856819.1:p.Cys397=
NM_001291940.2:c.-87G=	NP_001278869.1:n.-87G=
NM_000254.3:c.1022G= MANE Select	NP_000245.2:p.Cys341=