Canonical Allele Identifier: CA2487101850
Gene: MTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236880825_236880827delinsAGT , CM000663.2:g.236880825_236880827delinsAGT GRCh38
NC_000001.10:g.237044125_237044127delinsAGT , CM000663.1:g.237044125_237044127delinsAGT GRCh37
NC_000001.9:g.235110748_235110750delinsAGT NCBI36
NG_008959.1:g.90545_90547delinsAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000366577.10:c.2665_2667delinsAGT MANE Select ENSP00000355536.5:p.Ser889=
ENST00000535889.6:c.2512_2514delinsAGT ENSP00000441845.1:p.Ser838=
ENST00000650888.1:c.*1707_*1709delinsAGT ENSP00000498393.1:n.*1707_*1709delinsAGT
ENST00000651455.1:c.*1409_*1411delinsAGT ENSP00000498963.1:n.*1409_*1411delinsAGT
ENST00000674797.2:c.2317_2319delinsAGT ENSP00000502299.2:p.Ser773=
ENST00000679569.1:n.2979_2981delinsAGT
ENST00000679842.1:c.2476_2478delinsAGT ENSP00000506109.1:p.Ser826=
ENST00000680454.1:n.3109_3111delinsAGT
ENST00000681102.1:c.2485_2487delinsAGT ENSP00000505600.1:p.Ser829=
ENST00000681177.1:c.2227_2229delinsAGT ENSP00000506327.1:p.Ser743=
ENST00000681937.1:n.2859_2861delinsAGT
ENST00000366576.3:c.1327_1329delinsAGT ENSP00000355535.3:p.Ser443=
ENST00000366577.9:c.2665_2667delinsAGT ENSP00000355536.5:p.Ser889=
ENST00000535889.5:c.2512_2514delinsAGT ENSP00000441845.1:p.Ser838=
NM_000254.2:c.2665_2667delinsAGT NP_000245.2:p.Ser889=
NM_001291939.1:c.2512_2514delinsAGT NP_001278868.1:p.Ser838=
NM_001291940.1:c.1444_1446delinsAGT NP_001278869.1:p.Ser482=
XM_005273141.3:c.2662_2664delinsAGT XP_005273198.1:p.Ser888=
XM_006711769.2:c.2665_2667delinsAGT XP_006711832.1:p.Ser889=
XM_006711770.1:c.1729_1731delinsAGT XP_006711833.1:p.Ser577=
XM_011544193.1:c.2476_2478delinsAGT XP_011542495.1:p.Ser826=
XM_011544194.1:c.2833_2835delinsAGT XP_011542496.1:p.Ser945=
XM_005273141.5:c.2662_2664delinsAGT XP_005273198.1:p.Ser888=
XM_006711770.3:c.1729_1731delinsAGT XP_006711833.1:p.Ser577=
XM_011544194.3:c.2833_2835delinsAGT XP_011542496.1:p.Ser945=
XM_017001329.2:c.2680_2682delinsAGT XP_016856818.1:p.Ser894=
XM_017001330.2:c.2644_2646delinsAGT XP_016856819.1:p.Ser882=
NM_001291940.2:c.1444_1446delinsAGT NP_001278869.1:p.Ser482=
NM_000254.3:c.2665_2667delinsAGT MANE Select NP_000245.2:p.Ser889=