Canonical Allele Identifier: CA345384360

Gene: MTR

Linked Data

• COSMIC: COSM6398999
• MyVariant Identifiers: chr1:g.237048427C>A (hg19) ; chr1:g.236885127C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.2683C>A MANE Select	ENSP00000355536.5:p.Gln895Lys
ENST00000535889.6:c.2530C>A	ENSP00000441845.1:p.Gln844Lys
ENST00000650888.1:c.*1725C>A	ENSP00000498393.1:n.*1725C>A
ENST00000651455.1:c.*1427C>A	ENSP00000498963.1:n.*1427C>A
ENST00000674797.2:c.2335C>A	ENSP00000502299.2:p.Gln779Lys
ENST00000679569.1:n.2997C>A
ENST00000679842.1:c.2494C>A	ENSP00000506109.1:p.Gln832Lys
ENST00000680454.1:n.3127C>A
ENST00000681102.1:c.2503C>A	ENSP00000505600.1:p.Gln835Lys
ENST00000681177.1:c.2245C>A	ENSP00000506327.1:p.Gln749Lys
ENST00000681937.1:n.2877C>A
ENST00000366576.3:c.1345C>A	ENSP00000355535.3:p.Gln449Lys
ENST00000366577.9:c.2683C>A	ENSP00000355536.5:p.Gln895Lys
ENST00000535889.5:c.2530C>A	ENSP00000441845.1:p.Gln844Lys
NM_000254.2:c.2683C>A	NP_000245.2:p.Gln895Lys
NM_001291939.1:c.2530C>A	NP_001278868.1:p.Gln844Lys
NM_001291940.1:c.1462C>A	NP_001278869.1:p.Gln488Lys
XM_005273141.3:c.2680C>A	XP_005273198.1:p.Gln894Lys
XM_006711769.2:c.2683C>A	XP_006711832.1:p.Gln895Lys
XM_006711770.1:c.1747C>A	XP_006711833.1:p.Gln583Lys
XM_011544193.1:c.2494C>A	XP_011542495.1:p.Gln832Lys
XM_011544194.1:c.2851C>A	XP_011542496.1:p.Gln951Lys
XM_005273141.5:c.2680C>A	XP_005273198.1:p.Gln894Lys
XM_006711770.3:c.1747C>A	XP_006711833.1:p.Gln583Lys
XM_011544194.3:c.2851C>A	XP_011542496.1:p.Gln951Lys
XM_017001329.2:c.2698C>A	XP_016856818.1:p.Gln900Lys
XM_017001330.2:c.2662C>A	XP_016856819.1:p.Gln888Lys
NM_001291940.2:c.1462C>A	NP_001278869.1:p.Gln488Lys
NM_000254.3:c.2683C>A MANE Select	NP_000245.2:p.Gln895Lys