Canonical Allele Identifier: CA345384362

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237048427C>G (hg19) ; chr1:g.236885127C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236885127C>G , CM000663.2:g.236885127C>G	GRCh38
NC_000001.10:g.237048427C>G , CM000663.1:g.237048427C>G	GRCh37
NC_000001.9:g.235115050C>G	NCBI36
NG_008959.1:g.94847C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000366577.10:c.2683C>G MANE Select	ENSP00000355536.5:p.Gln895Glu
ENST00000535889.6:c.2530C>G	ENSP00000441845.1:p.Gln844Glu
ENST00000650888.1:c.*1725C>G	ENSP00000498393.1:n.*1725C>G
ENST00000651455.1:c.*1427C>G	ENSP00000498963.1:n.*1427C>G
ENST00000674797.2:c.2335C>G	ENSP00000502299.2:p.Gln779Glu
ENST00000679569.1:n.2997C>G
ENST00000679842.1:c.2494C>G	ENSP00000506109.1:p.Gln832Glu
ENST00000680454.1:n.3127C>G
ENST00000681102.1:c.2503C>G	ENSP00000505600.1:p.Gln835Glu
ENST00000681177.1:c.2245C>G	ENSP00000506327.1:p.Gln749Glu
ENST00000681937.1:n.2877C>G
ENST00000366576.3:c.1345C>G	ENSP00000355535.3:p.Gln449Glu
ENST00000366577.9:c.2683C>G	ENSP00000355536.5:p.Gln895Glu
ENST00000535889.5:c.2530C>G	ENSP00000441845.1:p.Gln844Glu
NM_000254.2:c.2683C>G	NP_000245.2:p.Gln895Glu
NM_001291939.1:c.2530C>G	NP_001278868.1:p.Gln844Glu
NM_001291940.1:c.1462C>G	NP_001278869.1:p.Gln488Glu
XM_005273141.3:c.2680C>G	XP_005273198.1:p.Gln894Glu
XM_006711769.2:c.2683C>G	XP_006711832.1:p.Gln895Glu
XM_006711770.1:c.1747C>G	XP_006711833.1:p.Gln583Glu
XM_011544193.1:c.2494C>G	XP_011542495.1:p.Gln832Glu
XM_011544194.1:c.2851C>G	XP_011542496.1:p.Gln951Glu
XM_005273141.5:c.2680C>G	XP_005273198.1:p.Gln894Glu
XM_006711770.3:c.1747C>G	XP_006711833.1:p.Gln583Glu
XM_011544194.3:c.2851C>G	XP_011542496.1:p.Gln951Glu
XM_017001329.2:c.2698C>G	XP_016856818.1:p.Gln900Glu
XM_017001330.2:c.2662C>G	XP_016856819.1:p.Gln888Glu
NM_001291940.2:c.1462C>G	NP_001278869.1:p.Gln488Glu
NM_000254.3:c.2683C>G MANE Select	NP_000245.2:p.Gln895Glu