Canonical Allele Identifier: CA1144211075

Gene: MTR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236829317G= , CM000663.2:g.236829317G=	GRCh38
NC_000001.10:g.236992617G= , CM000663.1:g.236992617G=	GRCh37
NC_000001.9:g.235059240G=	NCBI36
NG_008959.1:g.39037G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.1075+49G= MANE Select	ENSP00000355536.5:n.1075+49G=
ENST00000535889.6:c.1075+49G=	ENSP00000441845.1:n.1075+49G=
ENST00000650888.1:c.*117+49G=	ENSP00000498393.1:n.*117+49G=
ENST00000651455.1:c.1075+49G=	ENSP00000498963.1:n.1075+49G=
ENST00000674797.2:c.727+49G=	ENSP00000502299.2:n.727+49G=
ENST00000679569.1:n.1389+49G=
ENST00000679842.1:c.1075+49G=	ENSP00000506109.1:n.1075+49G=
ENST00000680454.1:n.1519+49G=
ENST00000681102.1:c.1075+49G=	ENSP00000505600.1:n.1075+49G=
ENST00000681177.1:c.1075+49G=	ENSP00000506327.1:n.1075+49G=
ENST00000681937.1:n.1707+49G=
ENST00000366577.9:c.1075+49G=	ENSP00000355536.5:n.1075+49G=
ENST00000463959.1:n.1094+49G=
ENST00000535889.5:c.1075+49G=	ENSP00000441845.1:n.1075+49G=
NM_000254.2:c.1075+49G=	NP_000245.2:n.1075+49G=
NM_001291939.1:c.1075+49G=	NP_001278868.1:n.1075+49G=
NM_001291940.1:c.-34+49G=	NP_001278869.1:n.-34+49G=
XM_005273141.3:c.1072+49G=	XP_005273198.1:n.1072+49G=
XM_006711769.2:c.1075+49G=	XP_006711832.1:n.1075+49G=
XM_006711770.1:c.139+49G=	XP_006711833.1:n.139+49G=
XM_011544193.1:c.1075+49G=	XP_011542495.1:n.1075+49G=
XM_011544194.1:c.1243+49G=	XP_011542496.1:n.1243+49G=
XM_005273141.5:c.1072+49G=	XP_005273198.1:n.1072+49G=
XM_006711770.3:c.139+49G=	XP_006711833.1:n.139+49G=
XM_011544194.3:c.1243+49G=	XP_011542496.1:n.1243+49G=
XM_017001329.2:c.1243+49G=	XP_016856818.1:n.1243+49G=
XM_017001330.2:c.1243+49G=	XP_016856819.1:n.1243+49G=
NM_001291940.2:c.-34+49G=	NP_001278869.1:n.-34+49G=
NM_000254.3:c.1075+49G= MANE Select	NP_000245.2:n.1075+49G=