Canonical Allele Identifier: CA2574163103
Gene: MTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236885122_236885123del , CM000663.2:g.236885122_236885123del GRCh38
NC_000001.10:g.237048422_237048423del , CM000663.1:g.237048422_237048423del GRCh37
NC_000001.9:g.235115045_235115046del NCBI36
NG_008959.1:g.94842_94843del

Transcript Alleles

HGVS Amino-acid change
ENST00000366577.10:c.2678_2679del
ENST00000535889.6:c.2525_2526del
ENST00000650888.1:c.*1720_*1721del
ENST00000651455.1:c.*1422_*1423del
ENST00000674797.2:c.2330_2331del
ENST00000679569.1:n.2992_2993del
ENST00000679842.1:c.2489_2490del
ENST00000680454.1:n.3122_3123del
ENST00000681102.1:c.2498_2499del
ENST00000681177.1:c.2240_2241del
ENST00000681937.1:n.2872_2873del
ENST00000366576.3:c.1340_1341del
ENST00000366577.9:c.2678_2679del
ENST00000535889.5:c.2525_2526del
NM_000254.2:c.2678_2679del
NM_001291939.1:c.2525_2526del
NM_001291940.1:c.1457_1458del
XM_005273141.3:c.2675_2676del
XM_006711769.2:c.2678_2679del
XM_006711770.1:c.1742_1743del
XM_011544193.1:c.2489_2490del
XM_011544194.1:c.2846_2847del
XM_005273141.5:c.2675_2676del
XM_006711770.3:c.1742_1743del
XM_011544194.3:c.2846_2847del
XM_017001329.2:c.2693_2694del
XM_017001330.2:c.2657_2658del
NM_001291940.2:c.1457_1458del
NM_000254.3:c.2678_2679del