Canonical Allele Identifier: CA1139926213
Gene: MTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236885376G= , CM000663.2:g.236885376G= GRCh38
NC_000001.10:g.237048676G= , CM000663.1:g.237048676G= GRCh37
NC_000001.9:g.235115299G= NCBI36
NG_008959.1:g.95096G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366577.10:c.2775+157G= MANE Select ENSP00000355536.5:n.2775+157G=
ENST00000535889.6:c.2622+157G= ENSP00000441845.1:n.2622+157G=
ENST00000650888.1:c.*1817+157G= ENSP00000498393.1:n.*1817+157G=
ENST00000651455.1:c.*1519+157G= ENSP00000498963.1:n.*1519+157G=
ENST00000674797.2:c.2427+157G= ENSP00000502299.2:n.2427+157G=
ENST00000679569.1:n.3089+157G=
ENST00000679842.1:c.2586+157G= ENSP00000506109.1:n.2586+157G=
ENST00000680454.1:n.3219+157G=
ENST00000681102.1:c.2595+157G= ENSP00000505600.1:n.2595+157G=
ENST00000681177.1:c.2337+157G= ENSP00000506327.1:n.2337+157G=
ENST00000681937.1:n.2969+157G=
ENST00000366576.3:c.1437+157G= ENSP00000355535.3:n.1437+157G=
ENST00000366577.9:c.2775+157G= ENSP00000355536.5:n.2775+157G=
ENST00000535889.5:c.2622+157G= ENSP00000441845.1:n.2622+157G=
NM_000254.2:c.2775+157G= NP_000245.2:n.2775+157G=
NM_001291939.1:c.2622+157G= NP_001278868.1:n.2622+157G=
NM_001291940.1:c.1554+157G= NP_001278869.1:n.1554+157G=
XM_005273141.3:c.2772+157G= XP_005273198.1:n.2772+157G=
XM_006711769.2:c.2775+157G= XP_006711832.1:n.2775+157G=
XM_006711770.1:c.1839+157G= XP_006711833.1:n.1839+157G=
XM_011544193.1:c.2586+157G= XP_011542495.1:n.2586+157G=
XM_011544194.1:c.2943+157G= XP_011542496.1:n.2943+157G=
XM_005273141.5:c.2772+157G= XP_005273198.1:n.2772+157G=
XM_006711770.3:c.1839+157G= XP_006711833.1:n.1839+157G=
XM_011544194.3:c.2943+157G= XP_011542496.1:n.2943+157G=
XM_017001329.2:c.2790+157G= XP_016856818.1:n.2790+157G=
XM_017001330.2:c.2754+157G= XP_016856819.1:n.2754+157G=
NM_001291940.2:c.1554+157G= NP_001278869.1:n.1554+157G=
NM_000254.3:c.2775+157G= MANE Select NP_000245.2:n.2775+157G=