Canonical Allele Identifier: CA423811458

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237015841A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236852541A>G , CM000663.2:g.236852541A>G	GRCh38
NC_000001.10:g.237015841A>G , CM000663.1:g.237015841A>G	GRCh37
NC_000001.9:g.235082464A>G	NCBI36
NG_008959.1:g.62261A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.1716A>G MANE Select	ENSP00000355536.5:p.Arg572=
ENST00000535889.6:c.1716A>G	ENSP00000441845.1:p.Arg572=
ENST00000650888.1:c.*758A>G	ENSP00000498393.1:n.*758A>G
ENST00000651455.1:c.*460A>G	ENSP00000498963.1:n.*460A>G
ENST00000674797.2:c.1368A>G	ENSP00000502299.2:p.Arg456=
ENST00000679569.1:n.2030A>G
ENST00000679842.1:c.1716A>G	ENSP00000506109.1:p.Arg572=
ENST00000680454.1:n.2160A>G
ENST00000681102.1:c.1536A>G	ENSP00000505600.1:p.Arg512=
ENST00000681177.1:c.1516-7292A>G	ENSP00000506327.1:n.1516-7292A>G
ENST00000681937.1:n.2148-7292A>G
ENST00000366576.3:c.378A>G	ENSP00000355535.3:p.Arg126=
ENST00000366577.9:c.1716A>G	ENSP00000355536.5:p.Arg572=
ENST00000463959.1:n.1735A>G
ENST00000535889.5:c.1716A>G	ENSP00000441845.1:p.Arg572=
NM_000254.2:c.1716A>G	NP_000245.2:p.Arg572=
NM_001291939.1:c.1716A>G	NP_001278868.1:p.Arg572=
NM_001291940.1:c.495A>G	NP_001278869.1:p.Arg165=
XM_005273141.3:c.1713A>G	XP_005273198.1:p.Arg571=
XM_006711769.2:c.1716A>G	XP_006711832.1:p.Arg572=
XM_006711770.1:c.780A>G	XP_006711833.1:p.Arg260=
XM_011544193.1:c.1716A>G	XP_011542495.1:p.Arg572=
XM_011544194.1:c.1884A>G	XP_011542496.1:p.Arg628=
XM_005273141.5:c.1713A>G	XP_005273198.1:p.Arg571=
XM_006711770.3:c.780A>G	XP_006711833.1:p.Arg260=
XM_011544194.3:c.1884A>G	XP_011542496.1:p.Arg628=
XM_017001329.2:c.1884A>G	XP_016856818.1:p.Arg628=
XM_017001330.2:c.1884A>G	XP_016856819.1:p.Arg628=
NM_001291940.2:c.495A>G	NP_001278869.1:p.Arg165=
NM_000254.3:c.1716A>G MANE Select	NP_000245.2:p.Arg572=