Canonical Allele Identifier: CA2487103722

Gene: MTR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236885207T= , CM000663.2:g.236885207T=	GRCh38
NC_000001.10:g.237048507T= , CM000663.1:g.237048507T=	GRCh37
NC_000001.9:g.235115130T=	NCBI36
NG_008959.1:g.94927T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366577.10:c.2763T= MANE Select	ENSP00000355536.5:p.Tyr921=
ENST00000535889.6:c.2610T=	ENSP00000441845.1:p.Tyr870=
ENST00000650888.1:c.*1805T=	ENSP00000498393.1:n.*1805T=
ENST00000651455.1:c.*1507T=	ENSP00000498963.1:n.*1507T=
ENST00000674797.2:c.2415T=	ENSP00000502299.2:p.Tyr805=
ENST00000679569.1:n.3077T=
ENST00000679842.1:c.2574T=	ENSP00000506109.1:p.Tyr858=
ENST00000680454.1:n.3207T=
ENST00000681102.1:c.2583T=	ENSP00000505600.1:p.Tyr861=
ENST00000681177.1:c.2325T=	ENSP00000506327.1:p.Tyr775=
ENST00000681937.1:n.2957T=
ENST00000366576.3:c.1425T=	ENSP00000355535.3:p.Tyr475=
ENST00000366577.9:c.2763T=	ENSP00000355536.5:p.Tyr921=
ENST00000535889.5:c.2610T=	ENSP00000441845.1:p.Tyr870=
NM_000254.2:c.2763T=	NP_000245.2:p.Tyr921=
NM_001291939.1:c.2610T=	NP_001278868.1:p.Tyr870=
NM_001291940.1:c.1542T=	NP_001278869.1:p.Tyr514=
XM_005273141.3:c.2760T=	XP_005273198.1:p.Tyr920=
XM_006711769.2:c.2763T=	XP_006711832.1:p.Tyr921=
XM_006711770.1:c.1827T=	XP_006711833.1:p.Tyr609=
XM_011544193.1:c.2574T=	XP_011542495.1:p.Tyr858=
XM_011544194.1:c.2931T=	XP_011542496.1:p.Tyr977=
XM_005273141.5:c.2760T=	XP_005273198.1:p.Tyr920=
XM_006711770.3:c.1827T=	XP_006711833.1:p.Tyr609=
XM_011544194.3:c.2931T=	XP_011542496.1:p.Tyr977=
XM_017001329.2:c.2778T=	XP_016856818.1:p.Tyr926=
XM_017001330.2:c.2742T=	XP_016856819.1:p.Tyr914=
NM_001291940.2:c.1542T=	NP_001278869.1:p.Tyr514=
NM_000254.3:c.2763T= MANE Select	NP_000245.2:p.Tyr921=