Canonical Allele Identifier: CA345384363

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237048428A>G (hg19) ; chr1:g.236885128A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236885128A>G , CM000663.2:g.236885128A>G	GRCh38
NC_000001.10:g.237048428A>G , CM000663.1:g.237048428A>G	GRCh37
NC_000001.9:g.235115051A>G	NCBI36
NG_008959.1:g.94848A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.2684A>G MANE Select	ENSP00000355536.5:p.Gln895Arg
ENST00000535889.6:c.2531A>G	ENSP00000441845.1:p.Gln844Arg
ENST00000650888.1:c.*1726A>G	ENSP00000498393.1:n.*1726A>G
ENST00000651455.1:c.*1428A>G	ENSP00000498963.1:n.*1428A>G
ENST00000674797.2:c.2336A>G	ENSP00000502299.2:p.Gln779Arg
ENST00000679569.1:n.2998A>G
ENST00000679842.1:c.2495A>G	ENSP00000506109.1:p.Gln832Arg
ENST00000680454.1:n.3128A>G
ENST00000681102.1:c.2504A>G	ENSP00000505600.1:p.Gln835Arg
ENST00000681177.1:c.2246A>G	ENSP00000506327.1:p.Gln749Arg
ENST00000681937.1:n.2878A>G
ENST00000366576.3:c.1346A>G	ENSP00000355535.3:p.Gln449Arg
ENST00000366577.9:c.2684A>G	ENSP00000355536.5:p.Gln895Arg
ENST00000535889.5:c.2531A>G	ENSP00000441845.1:p.Gln844Arg
NM_000254.2:c.2684A>G	NP_000245.2:p.Gln895Arg
NM_001291939.1:c.2531A>G	NP_001278868.1:p.Gln844Arg
NM_001291940.1:c.1463A>G	NP_001278869.1:p.Gln488Arg
XM_005273141.3:c.2681A>G	XP_005273198.1:p.Gln894Arg
XM_006711769.2:c.2684A>G	XP_006711832.1:p.Gln895Arg
XM_006711770.1:c.1748A>G	XP_006711833.1:p.Gln583Arg
XM_011544193.1:c.2495A>G	XP_011542495.1:p.Gln832Arg
XM_011544194.1:c.2852A>G	XP_011542496.1:p.Gln951Arg
XM_005273141.5:c.2681A>G	XP_005273198.1:p.Gln894Arg
XM_006711770.3:c.1748A>G	XP_006711833.1:p.Gln583Arg
XM_011544194.3:c.2852A>G	XP_011542496.1:p.Gln951Arg
XM_017001329.2:c.2699A>G	XP_016856818.1:p.Gln900Arg
XM_017001330.2:c.2663A>G	XP_016856819.1:p.Gln888Arg
NM_001291940.2:c.1463A>G	NP_001278869.1:p.Gln488Arg
NM_000254.3:c.2684A>G MANE Select	NP_000245.2:p.Gln895Arg