Canonical Allele Identifier: CA1139895347

Gene: MTR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236885200A= , CM000663.2:g.236885200A=	GRCh38
NC_000001.10:g.237048500A= , CM000663.1:g.237048500A=	GRCh37
NC_000001.9:g.235115123A=	NCBI36
NG_008959.1:g.94920A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366577.10:c.2756A= MANE Select	ENSP00000355536.5:p.Asp919=
ENST00000535889.6:c.2603A=	ENSP00000441845.1:p.Asp868=
ENST00000650888.1:c.*1798A=	ENSP00000498393.1:n.*1798A=
ENST00000651455.1:c.*1500A=	ENSP00000498963.1:n.*1500A=
ENST00000674797.2:c.2408A=	ENSP00000502299.2:p.Asp803=
ENST00000679569.1:n.3070A=
ENST00000679842.1:c.2567A=	ENSP00000506109.1:p.Asp856=
ENST00000680454.1:n.3200A=
ENST00000681102.1:c.2576A=	ENSP00000505600.1:p.Asp859=
ENST00000681177.1:c.2318A=	ENSP00000506327.1:p.Asp773=
ENST00000681937.1:n.2950A=
ENST00000366576.3:c.1418A=	ENSP00000355535.3:p.Asp473=
ENST00000366577.9:c.2756A=	ENSP00000355536.5:p.Asp919=
ENST00000535889.5:c.2603A=	ENSP00000441845.1:p.Asp868=
NM_000254.2:c.2756A=	NP_000245.2:p.Asp919=
NM_001291939.1:c.2603A=	NP_001278868.1:p.Asp868=
NM_001291940.1:c.1535A=	NP_001278869.1:p.Asp512=
XM_005273141.3:c.2753A=	XP_005273198.1:p.Asp918=
XM_006711769.2:c.2756A=	XP_006711832.1:p.Asp919=
XM_006711770.1:c.1820A=	XP_006711833.1:p.Asp607=
XM_011544193.1:c.2567A=	XP_011542495.1:p.Asp856=
XM_011544194.1:c.2924A=	XP_011542496.1:p.Asp975=
XM_005273141.5:c.2753A=	XP_005273198.1:p.Asp918=
XM_006711770.3:c.1820A=	XP_006711833.1:p.Asp607=
XM_011544194.3:c.2924A=	XP_011542496.1:p.Asp975=
XM_017001329.2:c.2771A=	XP_016856818.1:p.Asp924=
XM_017001330.2:c.2735A=	XP_016856819.1:p.Asp912=
NM_001291940.2:c.1535A=	NP_001278869.1:p.Asp512=
NM_000254.3:c.2756A= MANE Select	NP_000245.2:p.Asp919=