Canonical Allele Identifier: CA2487103723

Gene: MTR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236885210G= , CM000663.2:g.236885210G=	GRCh38
NC_000001.10:g.237048510G= , CM000663.1:g.237048510G=	GRCh37
NC_000001.9:g.235115133G=	NCBI36
NG_008959.1:g.94930G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366577.10:c.2766G= MANE Select	ENSP00000355536.5:p.Glu922=
ENST00000535889.6:c.2613G=	ENSP00000441845.1:p.Glu871=
ENST00000650888.1:c.*1808G=	ENSP00000498393.1:n.*1808G=
ENST00000651455.1:c.*1510G=	ENSP00000498963.1:n.*1510G=
ENST00000674797.2:c.2418G=	ENSP00000502299.2:p.Glu806=
ENST00000679569.1:n.3080G=
ENST00000679842.1:c.2577G=	ENSP00000506109.1:p.Glu859=
ENST00000680454.1:n.3210G=
ENST00000681102.1:c.2586G=	ENSP00000505600.1:p.Glu862=
ENST00000681177.1:c.2328G=	ENSP00000506327.1:p.Glu776=
ENST00000681937.1:n.2960G=
ENST00000366576.3:c.1428G=	ENSP00000355535.3:p.Glu476=
ENST00000366577.9:c.2766G=	ENSP00000355536.5:p.Glu922=
ENST00000535889.5:c.2613G=	ENSP00000441845.1:p.Glu871=
NM_000254.2:c.2766G=	NP_000245.2:p.Glu922=
NM_001291939.1:c.2613G=	NP_001278868.1:p.Glu871=
NM_001291940.1:c.1545G=	NP_001278869.1:p.Glu515=
XM_005273141.3:c.2763G=	XP_005273198.1:p.Glu921=
XM_006711769.2:c.2766G=	XP_006711832.1:p.Glu922=
XM_006711770.1:c.1830G=	XP_006711833.1:p.Glu610=
XM_011544193.1:c.2577G=	XP_011542495.1:p.Glu859=
XM_011544194.1:c.2934G=	XP_011542496.1:p.Glu978=
XM_005273141.5:c.2763G=	XP_005273198.1:p.Glu921=
XM_006711770.3:c.1830G=	XP_006711833.1:p.Glu610=
XM_011544194.3:c.2934G=	XP_011542496.1:p.Glu978=
XM_017001329.2:c.2781G=	XP_016856818.1:p.Glu927=
XM_017001330.2:c.2745G=	XP_016856819.1:p.Glu915=
NM_001291940.2:c.1545G=	NP_001278869.1:p.Glu515=
NM_000254.3:c.2766G= MANE Select	NP_000245.2:p.Glu922=