Canonical Allele Identifier: CA1474153
Gene: MTR HGNC NCBI

Linked Data

dbSNP Id: rs775353270

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236852518del , CM000663.2:g.236852518del GRCh38
NC_000001.10:g.237015818del , CM000663.1:g.237015818del GRCh37
NC_000001.9:g.235082441del NCBI36
NG_008959.1:g.62238del

Transcript Alleles

HGVS Amino-acid Change
ENST00000366577.10:c.1696-3del MANE Select ENSP00000355536.5:n.1696-3del
ENST00000535889.6:c.1696-3del ENSP00000441845.1:n.1696-3del
ENST00000650888.1:c.*738-3del ENSP00000498393.1:n.*738-3del
ENST00000651455.1:c.*440-3del ENSP00000498963.1:n.*440-3del
ENST00000674797.2:c.1348-3del ENSP00000502299.2:n.1348-3del
ENST00000679569.1:n.2010-3del
ENST00000679842.1:c.1696-3del ENSP00000506109.1:n.1696-3del
ENST00000680454.1:n.2140-3del
ENST00000681102.1:c.1516-3del ENSP00000505600.1:n.1516-3del
ENST00000681177.1:c.1516-7315del ENSP00000506327.1:n.1516-7315del
ENST00000681937.1:n.2148-7315del
ENST00000366576.3:c.358-3del ENSP00000355535.3:n.358-3del
ENST00000366577.9:c.1696-3del ENSP00000355536.5:n.1696-3del
ENST00000463959.1:n.1715-3del
ENST00000535889.5:c.1696-3del ENSP00000441845.1:n.1696-3del
NM_000254.2:c.1696-3del NP_000245.2:n.1696-3del
NM_001291939.1:c.1696-3del NP_001278868.1:n.1696-3del
NM_001291940.1:c.475-3del NP_001278869.1:n.475-3del
XM_005273141.3:c.1693-3del XP_005273198.1:n.1693-3del
XM_006711769.2:c.1696-3del XP_006711832.1:n.1696-3del
XM_006711770.1:c.760-3del XP_006711833.1:n.760-3del
XM_011544193.1:c.1696-3del XP_011542495.1:n.1696-3del
XM_011544194.1:c.1864-3del XP_011542496.1:n.1864-3del
XM_005273141.5:c.1693-3del XP_005273198.1:n.1693-3del
XM_006711770.3:c.760-3del XP_006711833.1:n.760-3del
XM_011544194.3:c.1864-3del XP_011542496.1:n.1864-3del
XM_017001329.2:c.1864-3del XP_016856818.1:n.1864-3del
XM_017001330.2:c.1864-3del XP_016856819.1:n.1864-3del
NM_001291940.2:c.475-3del NP_001278869.1:n.475-3del
NM_000254.3:c.1696-3del MANE Select NP_000245.2:n.1696-3del