Canonical Allele Identifier: CA1143621387

Gene: MTR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236852914T= , CM000663.2:g.236852914T=	GRCh38
NC_000001.10:g.237016214T= , CM000663.1:g.237016214T=	GRCh37
NC_000001.9:g.235082837T=	NCBI36
NG_008959.1:g.62634T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.1813-34T= MANE Select	ENSP00000355536.5:n.1813-34T=
ENST00000535889.6:c.1813-34T=	ENSP00000441845.1:n.1813-34T=
ENST00000650888.1:c.*855-34T=	ENSP00000498393.1:n.*855-34T=
ENST00000651455.1:c.*557-34T=	ENSP00000498963.1:n.*557-34T=
ENST00000674797.2:c.1465-34T=	ENSP00000502299.2:n.1465-34T=
ENST00000679569.1:n.2127-34T=
ENST00000679842.1:c.1813-34T=	ENSP00000506109.1:n.1813-34T=
ENST00000680454.1:n.2257-34T=
ENST00000681102.1:c.1633-34T=	ENSP00000505600.1:n.1633-34T=
ENST00000681177.1:c.1516-6919T=	ENSP00000506327.1:n.1516-6919T=
ENST00000681937.1:n.2148-6919T=
ENST00000366576.3:c.475-34T=	ENSP00000355535.3:n.475-34T=
ENST00000366577.9:c.1813-34T=	ENSP00000355536.5:n.1813-34T=
ENST00000463959.1:n.1832-34T=
ENST00000535889.5:c.1813-34T=	ENSP00000441845.1:n.1813-34T=
NM_000254.2:c.1813-34T=	NP_000245.2:n.1813-34T=
NM_001291939.1:c.1813-34T=	NP_001278868.1:n.1813-34T=
NM_001291940.1:c.592-34T=	NP_001278869.1:n.592-34T=
XM_005273141.3:c.1810-34T=	XP_005273198.1:n.1810-34T=
XM_006711769.2:c.1813-34T=	XP_006711832.1:n.1813-34T=
XM_006711770.1:c.877-34T=	XP_006711833.1:n.877-34T=
XM_011544193.1:c.1813-34T=	XP_011542495.1:n.1813-34T=
XM_011544194.1:c.1981-34T=	XP_011542496.1:n.1981-34T=
XM_005273141.5:c.1810-34T=	XP_005273198.1:n.1810-34T=
XM_006711770.3:c.877-34T=	XP_006711833.1:n.877-34T=
XM_011544194.3:c.1981-34T=	XP_011542496.1:n.1981-34T=
XM_017001329.2:c.1981-34T=	XP_016856818.1:n.1981-34T=
XM_017001330.2:c.1981-34T=	XP_016856819.1:n.1981-34T=
NM_001291940.2:c.592-34T=	NP_001278869.1:n.592-34T=
NM_000254.3:c.1813-34T= MANE Select	NP_000245.2:n.1813-34T=