Canonical Allele Identifier: CA1141581489

Gene: MTR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236885202C= , CM000663.2:g.236885202C=	GRCh38
NC_000001.10:g.237048502C= , CM000663.1:g.237048502C=	GRCh37
NC_000001.9:g.235115125C=	NCBI36
NG_008959.1:g.94922C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366577.10:c.2758C= MANE Select	ENSP00000355536.5:p.His920=
ENST00000535889.6:c.2605C=	ENSP00000441845.1:p.His869=
ENST00000650888.1:c.*1800C=	ENSP00000498393.1:n.*1800C=
ENST00000651455.1:c.*1502C=	ENSP00000498963.1:n.*1502C=
ENST00000674797.2:c.2410C=	ENSP00000502299.2:p.His804=
ENST00000679569.1:n.3072C=
ENST00000679842.1:c.2569C=	ENSP00000506109.1:p.His857=
ENST00000680454.1:n.3202C=
ENST00000681102.1:c.2578C=	ENSP00000505600.1:p.His860=
ENST00000681177.1:c.2320C=	ENSP00000506327.1:p.His774=
ENST00000681937.1:n.2952C=
ENST00000366576.3:c.1420C=	ENSP00000355535.3:p.His474=
ENST00000366577.9:c.2758C=	ENSP00000355536.5:p.His920=
ENST00000535889.5:c.2605C=	ENSP00000441845.1:p.His869=
NM_000254.2:c.2758C=	NP_000245.2:p.His920=
NM_001291939.1:c.2605C=	NP_001278868.1:p.His869=
NM_001291940.1:c.1537C=	NP_001278869.1:p.His513=
XM_005273141.3:c.2755C=	XP_005273198.1:p.His919=
XM_006711769.2:c.2758C=	XP_006711832.1:p.His920=
XM_006711770.1:c.1822C=	XP_006711833.1:p.His608=
XM_011544193.1:c.2569C=	XP_011542495.1:p.His857=
XM_011544194.1:c.2926C=	XP_011542496.1:p.His976=
XM_005273141.5:c.2755C=	XP_005273198.1:p.His919=
XM_006711770.3:c.1822C=	XP_006711833.1:p.His608=
XM_011544194.3:c.2926C=	XP_011542496.1:p.His976=
XM_017001329.2:c.2773C=	XP_016856818.1:p.His925=
XM_017001330.2:c.2737C=	XP_016856819.1:p.His913=
NM_001291940.2:c.1537C=	NP_001278869.1:p.His513=
NM_000254.3:c.2758C= MANE Select	NP_000245.2:p.His920=