Canonical Allele Identifier: CA2487101859
Gene: MTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236880842_236880865delinsTGGGTGACCTTACATTTTATTCCA , CM000663.2:g.236880842_236880865delinsTGGGTGACCTTACATTTTATTCCA GRCh38
NC_000001.10:g.237044142_237044165delinsTGGGTGACCTTACATTTTATTCCA , CM000663.1:g.237044142_237044165delinsTGGGTGACCTTACATTTTATTCCA GRCh37
NC_000001.9:g.235110765_235110788delinsTGGGTGACCTTACATTTTATTCCA NCBI36
NG_008959.1:g.90562_90585delinsTGGGTGACCTTACATTTTATTCCA

Transcript Alleles

HGVS Amino-acid change
ENST00000366577.10:c.2676+6_2676+29delinsTGGGTGACCTTACATTTTATTCCA MANE Select ENSP00000355536.5:n.2676+6_2676+29delinsT...
ENST00000535889.6:c.2523+6_2523+29delinsTGGGTGACCTTACATTTTATTCCA ENSP00000441845.1:n.2523+6_2523+29delinsT...
ENST00000650888.1:c.*1718+6_*1718+29delinsTGGGTGACCTTACATTTTATTCCA ENSP00000498393.1:n.*1718+6_*1718+29delin...
ENST00000651455.1:c.*1420+6_*1420+29delinsTGGGTGACCTTACATTTTATTCCA ENSP00000498963.1:n.*1420+6_*1420+29delin...
ENST00000674797.2:c.2328+6_2328+29delinsTGGGTGACCTTACATTTTATTCCA ENSP00000502299.2:n.2328+6_2328+29delinsT...
ENST00000679569.1:n.2990+6_2990+29delinsTGGGTGACCTTACATTTTATTCCA
ENST00000679842.1:c.2487+6_2487+29delinsTGGGTGACCTTACATTTTATTCCA ENSP00000506109.1:n.2487+6_2487+29delinsT...
ENST00000680454.1:n.3120+6_3120+29delinsTGGGTGACCTTACATTTTATTCCA
ENST00000681102.1:c.2496+6_2496+29delinsTGGGTGACCTTACATTTTATTCCA ENSP00000505600.1:n.2496+6_2496+29delinsT...
ENST00000681177.1:c.2238+6_2238+29delinsTGGGTGACCTTACATTTTATTCCA ENSP00000506327.1:n.2238+6_2238+29delinsT...
ENST00000681937.1:n.2870+6_2870+29delinsTGGGTGACCTTACATTTTATTCCA
ENST00000366576.3:c.1338+6_1338+29delinsTGGGTGACCTTACATTTTATTCCA ENSP00000355535.3:n.1338+6_1338+29delinsT...
ENST00000366577.9:c.2676+6_2676+29delinsTGGGTGACCTTACATTTTATTCCA ENSP00000355536.5:n.2676+6_2676+29delinsT...
ENST00000535889.5:c.2523+6_2523+29delinsTGGGTGACCTTACATTTTATTCCA ENSP00000441845.1:n.2523+6_2523+29delinsT...
NM_000254.2:c.2676+6_2676+29delinsTGGGTGACCTTACATTTTATTCCA NP_000245.2:n.2676+6_2676+29delinsTGGGTGA...
NM_001291939.1:c.2523+6_2523+29delinsTGGGTGACCTTACATTTTATTCCA NP_001278868.1:n.2523+6_2523+29delinsTGGG...
NM_001291940.1:c.1455+6_1455+29delinsTGGGTGACCTTACATTTTATTCCA NP_001278869.1:n.1455+6_1455+29delinsTGGG...
XM_005273141.3:c.2673+6_2673+29delinsTGGGTGACCTTACATTTTATTCCA XP_005273198.1:n.2673+6_2673+29delinsTGGG...
XM_006711769.2:c.2676+6_2676+29delinsTGGGTGACCTTACATTTTATTCCA XP_006711832.1:n.2676+6_2676+29delinsTGGG...
XM_006711770.1:c.1740+6_1740+29delinsTGGGTGACCTTACATTTTATTCCA XP_006711833.1:n.1740+6_1740+29delinsTGGG...
XM_011544193.1:c.2487+6_2487+29delinsTGGGTGACCTTACATTTTATTCCA XP_011542495.1:n.2487+6_2487+29delinsTGGG...
XM_011544194.1:c.2844+6_2844+29delinsTGGGTGACCTTACATTTTATTCCA XP_011542496.1:n.2844+6_2844+29delinsTGGG...
XM_005273141.5:c.2673+6_2673+29delinsTGGGTGACCTTACATTTTATTCCA XP_005273198.1:n.2673+6_2673+29delinsTGGG...
XM_006711770.3:c.1740+6_1740+29delinsTGGGTGACCTTACATTTTATTCCA XP_006711833.1:n.1740+6_1740+29delinsTGGG...
XM_011544194.3:c.2844+6_2844+29delinsTGGGTGACCTTACATTTTATTCCA XP_011542496.1:n.2844+6_2844+29delinsTGGG...
XM_017001329.2:c.2691+6_2691+29delinsTGGGTGACCTTACATTTTATTCCA XP_016856818.1:n.2691+6_2691+29delinsTGGG...
XM_017001330.2:c.2655+6_2655+29delinsTGGGTGACCTTACATTTTATTCCA XP_016856819.1:n.2655+6_2655+29delinsTGGG...
NM_001291940.2:c.1455+6_1455+29delinsTGGGTGACCTTACATTTTATTCCA NP_001278869.1:n.1455+6_1455+29delinsTGGG...
NM_000254.3:c.2676+6_2676+29delinsTGGGTGACCTTACATTTTATTCCA MANE Select NP_000245.2:n.2676+6_2676+29delinsTGGGTGA...