Canonical Allele Identifier: CA2487103654

Gene: MTR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236884968T= , CM000663.2:g.236884968T=	GRCh38
NC_000001.10:g.237048268T= , CM000663.1:g.237048268T=	GRCh37
NC_000001.9:g.235114891T=	NCBI36
NG_008959.1:g.94688T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.2677-153T= MANE Select	ENSP00000355536.5:n.2677-153T=
ENST00000535889.6:c.2524-153T=	ENSP00000441845.1:n.2524-153T=
ENST00000650888.1:c.*1719-153T=	ENSP00000498393.1:n.*1719-153T=
ENST00000651455.1:c.*1421-153T=	ENSP00000498963.1:n.*1421-153T=
ENST00000674797.2:c.2329-153T=	ENSP00000502299.2:n.2329-153T=
ENST00000679569.1:n.2991-153T=
ENST00000679842.1:c.2488-153T=	ENSP00000506109.1:n.2488-153T=
ENST00000680454.1:n.3121-153T=
ENST00000681102.1:c.2497-153T=	ENSP00000505600.1:n.2497-153T=
ENST00000681177.1:c.2239-153T=	ENSP00000506327.1:n.2239-153T=
ENST00000681937.1:n.2871-153T=
ENST00000366576.3:c.1339-153T=	ENSP00000355535.3:n.1339-153T=
ENST00000366577.9:c.2677-153T=	ENSP00000355536.5:n.2677-153T=
ENST00000535889.5:c.2524-153T=	ENSP00000441845.1:n.2524-153T=
NM_000254.2:c.2677-153T=	NP_000245.2:n.2677-153T=
NM_001291939.1:c.2524-153T=	NP_001278868.1:n.2524-153T=
NM_001291940.1:c.1456-153T=	NP_001278869.1:n.1456-153T=
XM_005273141.3:c.2674-153T=	XP_005273198.1:n.2674-153T=
XM_006711769.2:c.2677-153T=	XP_006711832.1:n.2677-153T=
XM_006711770.1:c.1741-153T=	XP_006711833.1:n.1741-153T=
XM_011544193.1:c.2488-153T=	XP_011542495.1:n.2488-153T=
XM_011544194.1:c.2845-153T=	XP_011542496.1:n.2845-153T=
XM_005273141.5:c.2674-153T=	XP_005273198.1:n.2674-153T=
XM_006711770.3:c.1741-153T=	XP_006711833.1:n.1741-153T=
XM_011544194.3:c.2845-153T=	XP_011542496.1:n.2845-153T=
XM_017001329.2:c.2692-153T=	XP_016856818.1:n.2692-153T=
XM_017001330.2:c.2656-153T=	XP_016856819.1:n.2656-153T=
NM_001291940.2:c.1456-153T=	NP_001278869.1:n.1456-153T=
NM_000254.3:c.2677-153T= MANE Select	NP_000245.2:n.2677-153T=