Canonical Allele Identifier: CA2651187353
Gene: MTR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236852809C>A , CM000663.2:g.236852809C>A GRCh38
NC_000001.10:g.237016109C>A , CM000663.1:g.237016109C>A GRCh37
NC_000001.9:g.235082732C>A NCBI36
NG_008959.1:g.62529C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000366577.10:c.1813-139C>A MANE Select ENSP00000355536.5:n.1813-139C>A
ENST00000535889.6:c.1813-139C>A ENSP00000441845.1:n.1813-139C>A
ENST00000650888.1:c.*855-139C>A ENSP00000498393.1:n.*855-139C>A
ENST00000651455.1:c.*557-139C>A ENSP00000498963.1:n.*557-139C>A
ENST00000674797.2:c.1465-139C>A ENSP00000502299.2:n.1465-139C>A
ENST00000679569.1:n.2127-139C>A
ENST00000679842.1:c.1813-139C>A ENSP00000506109.1:n.1813-139C>A
ENST00000680454.1:n.2257-139C>A
ENST00000681102.1:c.1633-139C>A ENSP00000505600.1:n.1633-139C>A
ENST00000681177.1:c.1516-7024C>A ENSP00000506327.1:n.1516-7024C>A
ENST00000681937.1:n.2148-7024C>A
ENST00000366576.3:c.475-139C>A ENSP00000355535.3:n.475-139C>A
ENST00000366577.9:c.1813-139C>A ENSP00000355536.5:n.1813-139C>A
ENST00000463959.1:n.1832-139C>A
ENST00000535889.5:c.1813-139C>A ENSP00000441845.1:n.1813-139C>A
NM_000254.2:c.1813-139C>A NP_000245.2:n.1813-139C>A
NM_001291939.1:c.1813-139C>A NP_001278868.1:n.1813-139C>A
NM_001291940.1:c.592-139C>A NP_001278869.1:n.592-139C>A
XM_005273141.3:c.1810-139C>A XP_005273198.1:n.1810-139C>A
XM_006711769.2:c.1813-139C>A XP_006711832.1:n.1813-139C>A
XM_006711770.1:c.877-139C>A XP_006711833.1:n.877-139C>A
XM_011544193.1:c.1813-139C>A XP_011542495.1:n.1813-139C>A
XM_011544194.1:c.1981-139C>A XP_011542496.1:n.1981-139C>A
XM_005273141.5:c.1810-139C>A XP_005273198.1:n.1810-139C>A
XM_006711770.3:c.877-139C>A XP_006711833.1:n.877-139C>A
XM_011544194.3:c.1981-139C>A XP_011542496.1:n.1981-139C>A
XM_017001329.2:c.1981-139C>A XP_016856818.1:n.1981-139C>A
XM_017001330.2:c.1981-139C>A XP_016856819.1:n.1981-139C>A
NM_001291940.2:c.592-139C>A NP_001278869.1:n.592-139C>A
NM_000254.3:c.1813-139C>A MANE Select NP_000245.2:n.1813-139C>A