Canonical Allele Identifier: CA1525801378
Gene: MTRR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.7877965G= , CM000667.2:g.7877965G= GRCh38
NC_000005.9:g.7878078G= , CM000667.1:g.7878078G= GRCh37
NC_000005.8:g.7931078G= NCBI36
NG_008856.1:g.13862G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000440940.7:c.423G= MANE Select ENSP00000402510.2:p.Pro141=
ENST00000264668.6:c.504G= ENSP00000264668.2:p.Pro168=
ENST00000440940.6:c.423G= ENSP00000402510.2:p.Pro141=
ENST00000502509.5:n.638G=
ENST00000502550.5:c.423G= ENSP00000424599.1:p.Pro141=
ENST00000503550.5:c.*358G= ENSP00000424644.1:n.*358G=
ENST00000508047.5:c.476G=
ENST00000508890.1:n.236G=
ENST00000510279.5:c.*92G= ENSP00000427200.1:n.*92G=
ENST00000510525.5:c.448G=
ENST00000511461.5:c.336G=
ENST00000513439.5:c.*130G= ENSP00000426710.1:n.*130G=
ENST00000514220.5:c.208G=
ENST00000514369.5:c.*87G= ENSP00000426132.1:n.*87G=
NM_002454.2:c.423G= NP_002445.2:p.Pro141=
NM_024010.2:c.504G= NP_076915.2:p.Pro168=
XM_006714474.2:c.504G= XP_006714537.1:p.Pro168=
XM_011514043.1:c.504G= XP_011512345.1:p.Pro168=
XM_011514044.1:c.423G= XP_011512346.1:p.Pro141=
XM_011514045.1:c.504G= XP_011512347.1:p.Pro168=
XR_241702.1:n.526G=
XR_241703.1:n.519G=
XR_925614.1:n.526G=
XR_925615.1:n.526G=
NM_001364440.1:c.423G= NP_001351369.1:p.Pro141=
NM_001364441.1:c.423G= NP_001351370.1:p.Pro141=
NM_001364442.1:c.423G= NP_001351371.1:p.Pro141=
NM_024010.3:c.423G= NP_076915.3:p.Pro141=
NR_134480.1:n.546G=
NR_134481.1:n.560G=
NR_134482.1:n.406G=
NR_157168.1:n.476G=
NR_157169.1:n.336G=
NR_157170.1:n.362G=
NR_157171.1:n.336G=
NR_157172.1:n.362G=
NR_157173.1:n.490G=
NR_157174.1:n.362G=
NR_157175.1:n.516G=
NR_157176.1:n.516G=
NR_157177.1:n.511G=
NR_157178.1:n.516G=
XM_024446063.1:c.468G= XP_024301831.1:p.Pro156=
XM_024446064.1:c.423G= XP_024301832.1:p.Pro141=
XR_001742071.1:n.526G=
XR_001742072.1:n.526G=
XR_001742074.1:n.526G=
XR_001742075.1:n.526G=
XR_001742076.1:n.526G=
XR_001742077.1:n.526G=
NM_001364440.2:c.423G= NP_001351369.1:p.Pro141=
NM_001364441.2:c.423G= NP_001351370.1:p.Pro141=
NM_001364442.2:c.423G= NP_001351371.1:p.Pro141=
NM_002454.3:c.423G= MANE Select NP_002445.2:p.Pro141=
NM_024010.4:c.423G= NP_076915.3:p.Pro141=
NR_134480.2:n.502G=
NR_134481.2:n.516G=
NR_134482.2:n.362G=
NR_157168.2:n.476G=
NR_157169.2:n.336G=
NR_157170.2:n.362G=
NR_157171.2:n.336G=
NR_157172.2:n.362G=
NR_157173.2:n.490G=
NR_157174.2:n.362G=
NR_157175.2:n.516G=
NR_157176.2:n.516G=
NR_157177.2:n.511G=
NR_157178.2:n.516G=