Canonical Allele Identifier: CA2487090353

Gene: MTR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236852596C= , CM000663.2:g.236852596C=	GRCh38
NC_000001.10:g.237015896C= , CM000663.1:g.237015896C=	GRCh37
NC_000001.9:g.235082519C=	NCBI36
NG_008959.1:g.62316C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.1771C= MANE Select	ENSP00000355536.5:p.Arg591=
ENST00000535889.6:c.1771C=	ENSP00000441845.1:p.Arg591=
ENST00000650888.1:c.*813C=	ENSP00000498393.1:n.*813C=
ENST00000651455.1:c.*515C=	ENSP00000498963.1:n.*515C=
ENST00000674797.2:c.1423C=	ENSP00000502299.2:p.Arg475=
ENST00000679569.1:n.2085C=
ENST00000679842.1:c.1771C=	ENSP00000506109.1:p.Arg591=
ENST00000680454.1:n.2215C=
ENST00000681102.1:c.1591C=	ENSP00000505600.1:p.Arg531=
ENST00000681177.1:c.1516-7237C=	ENSP00000506327.1:n.1516-7237C=
ENST00000681937.1:n.2148-7237C=
ENST00000366576.3:c.433C=	ENSP00000355535.3:p.Arg145=
ENST00000366577.9:c.1771C=	ENSP00000355536.5:p.Arg591=
ENST00000463959.1:n.1790C=
ENST00000535889.5:c.1771C=	ENSP00000441845.1:p.Arg591=
NM_000254.2:c.1771C=	NP_000245.2:p.Arg591=
NM_001291939.1:c.1771C=	NP_001278868.1:p.Arg591=
NM_001291940.1:c.550C=	NP_001278869.1:p.Arg184=
XM_005273141.3:c.1768C=	XP_005273198.1:p.Arg590=
XM_006711769.2:c.1771C=	XP_006711832.1:p.Arg591=
XM_006711770.1:c.835C=	XP_006711833.1:p.Arg279=
XM_011544193.1:c.1771C=	XP_011542495.1:p.Arg591=
XM_011544194.1:c.1939C=	XP_011542496.1:p.Arg647=
XM_005273141.5:c.1768C=	XP_005273198.1:p.Arg590=
XM_006711770.3:c.835C=	XP_006711833.1:p.Arg279=
XM_011544194.3:c.1939C=	XP_011542496.1:p.Arg647=
XM_017001329.2:c.1939C=	XP_016856818.1:p.Arg647=
XM_017001330.2:c.1939C=	XP_016856819.1:p.Arg647=
NM_001291940.2:c.550C=	NP_001278869.1:p.Arg184=
NM_000254.3:c.1771C= MANE Select	NP_000245.2:p.Arg591=