Canonical Allele Identifier: CA2698361994
Gene: MTR HGNC NCBI

Linked Data

dbSNP Id: rs2103116836

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236829139_236829143del , CM000663.2:g.236829139_236829143del GRCh38
NC_000001.10:g.236992439_236992443del , CM000663.1:g.236992439_236992443del GRCh37
NC_000001.9:g.235059062_235059066del NCBI36
NG_008959.1:g.38859_38863del

Transcript Alleles

HGVS Amino-acid Change
ENST00000366577.10:c.996-50_996-46del MANE Select ENSP00000355536.5:n.996-50_996-46del
ENST00000535889.6:c.996-50_996-46del ENSP00000441845.1:n.996-50_996-46del
ENST00000650888.1:c.*38-50_*38-46del ENSP00000498393.1:n.*38-50_*38-46del
ENST00000651455.1:c.996-50_996-46del ENSP00000498963.1:n.996-50_996-46del
ENST00000674797.2:c.648-50_648-46del ENSP00000502299.2:n.648-50_648-46del
ENST00000679569.1:n.1310-50_1310-46del
ENST00000679842.1:c.996-50_996-46del ENSP00000506109.1:n.996-50_996-46del
ENST00000680454.1:n.1440-50_1440-46del
ENST00000681102.1:c.996-50_996-46del ENSP00000505600.1:n.996-50_996-46del
ENST00000681177.1:c.996-50_996-46del ENSP00000506327.1:n.996-50_996-46del
ENST00000681937.1:n.1628-50_1628-46del
ENST00000366577.9:c.996-50_996-46del ENSP00000355536.5:n.996-50_996-46del
ENST00000463959.1:n.1015-50_1015-46del
ENST00000535889.5:c.996-50_996-46del ENSP00000441845.1:n.996-50_996-46del
NM_000254.2:c.996-50_996-46del NP_000245.2:n.996-50_996-46del
NM_001291939.1:c.996-50_996-46del NP_001278868.1:n.996-50_996-46del
NM_001291940.1:c.-113-50_-113-46del NP_001278869.1:n.-113-50_-113-46del
XM_005273141.3:c.993-50_993-46del XP_005273198.1:n.993-50_993-46del
XM_006711769.2:c.996-50_996-46del XP_006711832.1:n.996-50_996-46del
XM_006711770.1:c.60-50_60-46del XP_006711833.1:n.60-50_60-46del
XM_011544193.1:c.996-50_996-46del XP_011542495.1:n.996-50_996-46del
XM_011544194.1:c.1164-50_1164-46del XP_011542496.1:n.1164-50_1164-46del
XM_005273141.5:c.993-50_993-46del XP_005273198.1:n.993-50_993-46del
XM_006711770.3:c.60-50_60-46del XP_006711833.1:n.60-50_60-46del
XM_011544194.3:c.1164-50_1164-46del XP_011542496.1:n.1164-50_1164-46del
XM_017001329.2:c.1164-50_1164-46del XP_016856818.1:n.1164-50_1164-46del
XM_017001330.2:c.1164-50_1164-46del XP_016856819.1:n.1164-50_1164-46del
NM_001291940.2:c.-113-50_-113-46del NP_001278869.1:n.-113-50_-113-46del
NM_000254.3:c.996-50_996-46del MANE Select NP_000245.2:n.996-50_996-46del