Canonical Allele Identifier: CA1525801366
Gene: MTRR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.7877956G= , CM000667.2:g.7877956G= GRCh38
NC_000005.9:g.7878069G= , CM000667.1:g.7878069G= GRCh37
NC_000005.8:g.7931069G= NCBI36
NG_008856.1:g.13853G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000440940.7:c.414G= MANE Select ENSP00000402510.2:p.Val138=
ENST00000264668.6:c.495G= ENSP00000264668.2:p.Val165=
ENST00000440940.6:c.414G= ENSP00000402510.2:p.Val138=
ENST00000502509.5:n.629G=
ENST00000502550.5:c.414G= ENSP00000424599.1:p.Val138=
ENST00000503550.5:c.*349G= ENSP00000424644.1:n.*349G=
ENST00000508047.5:c.467G=
ENST00000508890.1:n.227G=
ENST00000510279.5:c.*83G= ENSP00000427200.1:n.*83G=
ENST00000510525.5:c.439G=
ENST00000511461.5:c.327G=
ENST00000513439.5:c.*121G= ENSP00000426710.1:n.*121G=
ENST00000514220.5:c.199G=
ENST00000514369.5:c.*78G= ENSP00000426132.1:n.*78G=
NM_002454.2:c.414G= NP_002445.2:p.Val138=
NM_024010.2:c.495G= NP_076915.2:p.Val165=
XM_006714474.2:c.495G= XP_006714537.1:p.Val165=
XM_011514043.1:c.495G= XP_011512345.1:p.Val165=
XM_011514044.1:c.414G= XP_011512346.1:p.Val138=
XM_011514045.1:c.495G= XP_011512347.1:p.Val165=
XR_241702.1:n.517G=
XR_241703.1:n.510G=
XR_925614.1:n.517G=
XR_925615.1:n.517G=
NM_001364440.1:c.414G= NP_001351369.1:p.Val138=
NM_001364441.1:c.414G= NP_001351370.1:p.Val138=
NM_001364442.1:c.414G= NP_001351371.1:p.Val138=
NM_024010.3:c.414G= NP_076915.3:p.Val138=
NR_134480.1:n.537G=
NR_134481.1:n.551G=
NR_134482.1:n.397G=
NR_157168.1:n.467G=
NR_157169.1:n.327G=
NR_157170.1:n.353G=
NR_157171.1:n.327G=
NR_157172.1:n.353G=
NR_157173.1:n.481G=
NR_157174.1:n.353G=
NR_157175.1:n.507G=
NR_157176.1:n.507G=
NR_157177.1:n.502G=
NR_157178.1:n.507G=
XM_024446063.1:c.459G= XP_024301831.1:p.Val153=
XM_024446064.1:c.414G= XP_024301832.1:p.Val138=
XR_001742071.1:n.517G=
XR_001742072.1:n.517G=
XR_001742074.1:n.517G=
XR_001742075.1:n.517G=
XR_001742076.1:n.517G=
XR_001742077.1:n.517G=
NM_001364440.2:c.414G= NP_001351369.1:p.Val138=
NM_001364441.2:c.414G= NP_001351370.1:p.Val138=
NM_001364442.2:c.414G= NP_001351371.1:p.Val138=
NM_002454.3:c.414G= MANE Select NP_002445.2:p.Val138=
NM_024010.4:c.414G= NP_076915.3:p.Val138=
NR_134480.2:n.493G=
NR_134481.2:n.507G=
NR_134482.2:n.353G=
NR_157168.2:n.467G=
NR_157169.2:n.327G=
NR_157170.2:n.353G=
NR_157171.2:n.327G=
NR_157172.2:n.353G=
NR_157173.2:n.481G=
NR_157174.2:n.353G=
NR_157175.2:n.507G=
NR_157176.2:n.507G=
NR_157177.2:n.502G=
NR_157178.2:n.507G=