Canonical Allele Identifier: CA1139969825
Gene: MTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236898898A= , CM000663.2:g.236898898A= GRCh38
NC_000001.10:g.237062198A= , CM000663.1:g.237062198A= GRCh37
NC_000001.9:g.235128821A= NCBI36
NG_008959.1:g.108618A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366577.10:c.*1254A= MANE Select ENSP00000355536.5:n.*1254A=
ENST00000470570.2:n.5782A=
ENST00000650888.1:c.*4094A= ENSP00000498393.1:n.*4094A=
ENST00000652483.1:n.376A=
ENST00000674797.2:c.*1254A= ENSP00000502299.2:n.*1254A=
ENST00000679569.1:n.8179A=
ENST00000680454.1:n.8309A=
ENST00000681813.1:n.895A=
ENST00000681937.1:n.5246A=
ENST00000366576.3:c.3714A= ENSP00000355535.3:n.3714A=
ENST00000366577.9:c.*1254A= ENSP00000355536.5:n.*1254A=
ENST00000470570.1:n.2664A=
ENST00000535889.5:c.*1254A= ENSP00000441845.1:n.*1254A=
NM_000254.2:c.*1254A= NP_000245.2:n.*1254A=
NM_001291939.1:c.*1254A= NP_001278868.1:n.*1254A=
NM_001291940.1:c.*1254A= NP_001278869.1:n.*1254A=
XM_005273141.3:c.*1254A= XP_005273198.1:n.*1254A=
XM_006711770.1:c.*1254A= XP_006711833.1:n.*1254A=
XM_011544193.1:c.*1254A= XP_011542495.1:n.*1254A=
XM_011544194.1:c.*1254A= XP_011542496.1:n.*1254A=
XM_005273141.5:c.*1254A= XP_005273198.1:n.*1254A=
XM_006711770.3:c.*1254A= XP_006711833.1:n.*1254A=
XM_011544194.3:c.*1254A= XP_011542496.1:n.*1254A=
XM_017001329.2:c.*1254A= XP_016856818.1:n.*1254A=
XM_017001330.2:c.*1254A= XP_016856819.1:n.*1254A=
NM_001291940.2:c.*1254A= NP_001278869.1:n.*1254A=
NM_000254.3:c.*1254A= MANE Select NP_000245.2:n.*1254A=