Canonical Allele Identifier: CA423811488

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237015883A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236852583A>T , CM000663.2:g.236852583A>T	GRCh38
NC_000001.10:g.237015883A>T , CM000663.1:g.237015883A>T	GRCh37
NC_000001.9:g.235082506A>T	NCBI36
NG_008959.1:g.62303A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000366577.10:c.1758A>T MANE Select	ENSP00000355536.5:p.Gly586=
ENST00000535889.6:c.1758A>T	ENSP00000441845.1:p.Gly586=
ENST00000650888.1:c.*800A>T	ENSP00000498393.1:n.*800A>T
ENST00000651455.1:c.*502A>T	ENSP00000498963.1:n.*502A>T
ENST00000674797.2:c.1410A>T	ENSP00000502299.2:p.Gly470=
ENST00000679569.1:n.2072A>T
ENST00000679842.1:c.1758A>T	ENSP00000506109.1:p.Gly586=
ENST00000680454.1:n.2202A>T
ENST00000681102.1:c.1578A>T	ENSP00000505600.1:p.Gly526=
ENST00000681177.1:c.1516-7250A>T	ENSP00000506327.1:n.1516-7250A>T
ENST00000681937.1:n.2148-7250A>T
ENST00000366576.3:c.420A>T	ENSP00000355535.3:p.Gly140=
ENST00000366577.9:c.1758A>T	ENSP00000355536.5:p.Gly586=
ENST00000463959.1:n.1777A>T
ENST00000535889.5:c.1758A>T	ENSP00000441845.1:p.Gly586=
NM_000254.2:c.1758A>T	NP_000245.2:p.Gly586=
NM_001291939.1:c.1758A>T	NP_001278868.1:p.Gly586=
NM_001291940.1:c.537A>T	NP_001278869.1:p.Gly179=
XM_005273141.3:c.1755A>T	XP_005273198.1:p.Gly585=
XM_006711769.2:c.1758A>T	XP_006711832.1:p.Gly586=
XM_006711770.1:c.822A>T	XP_006711833.1:p.Gly274=
XM_011544193.1:c.1758A>T	XP_011542495.1:p.Gly586=
XM_011544194.1:c.1926A>T	XP_011542496.1:p.Gly642=
XM_005273141.5:c.1755A>T	XP_005273198.1:p.Gly585=
XM_006711770.3:c.822A>T	XP_006711833.1:p.Gly274=
XM_011544194.3:c.1926A>T	XP_011542496.1:p.Gly642=
XM_017001329.2:c.1926A>T	XP_016856818.1:p.Gly642=
XM_017001330.2:c.1926A>T	XP_016856819.1:p.Gly642=
NM_001291940.2:c.537A>T	NP_001278869.1:p.Gly179=
NM_000254.3:c.1758A>T MANE Select	NP_000245.2:p.Gly586=