Canonical Allele Identifier: CA359157019
Gene: MTRR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.7878117A>C , CM000667.2:g.7878117A>C GRCh38
NC_000005.9:g.7878230A>C , CM000667.1:g.7878230A>C GRCh37
NC_000005.8:g.7931230A>C NCBI36
NG_008856.1:g.14014A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000440940.7:c.575A>C MANE Select ENSP00000402510.2:p.Glu192Ala
ENST00000264668.6:c.656A>C ENSP00000264668.2:p.Glu219Ala
ENST00000440940.6:c.575A>C ENSP00000402510.2:p.Glu192Ala
ENST00000510279.5:c.*244A>C ENSP00000427200.1:n.*244A>C
ENST00000510525.5:c.600A>C
ENST00000511461.5:c.488A>C
ENST00000513439.5:c.*282A>C ENSP00000426710.1:n.*282A>C
ENST00000514220.5:c.360A>C
ENST00000514369.5:c.*239A>C ENSP00000426132.1:n.*239A>C
NM_002454.2:c.575A>C NP_002445.2:p.Glu192Ala
NM_024010.2:c.656A>C NP_076915.2:p.Glu219Ala
XM_006714474.2:c.656A>C XP_006714537.1:p.Glu219Ala
XM_011514043.1:c.656A>C XP_011512345.1:p.Glu219Ala
XM_011514044.1:c.575A>C XP_011512346.1:p.Glu192Ala
XM_011514045.1:c.656A>C XP_011512347.1:p.Glu219Ala
XR_241702.1:n.678A>C
XR_241703.1:n.671A>C
XR_925614.1:n.678A>C
XR_925615.1:n.678A>C
NM_001364440.1:c.575A>C NP_001351369.1:p.Glu192Ala
NM_001364441.1:c.575A>C NP_001351370.1:p.Glu192Ala
NM_001364442.1:c.575A>C NP_001351371.1:p.Glu192Ala
NM_024010.3:c.575A>C NP_076915.3:p.Glu192Ala
NR_134480.1:n.698A>C
NR_134481.1:n.712A>C
NR_134482.1:n.558A>C
NR_157168.1:n.628A>C
NR_157169.1:n.488A>C
NR_157170.1:n.514A>C
NR_157171.1:n.488A>C
NR_157172.1:n.514A>C
NR_157173.1:n.642A>C
NR_157174.1:n.514A>C
NR_157175.1:n.668A>C
NR_157176.1:n.668A>C
NR_157177.1:n.663A>C
NR_157178.1:n.668A>C
XM_024446063.1:c.620A>C XP_024301831.1:p.Glu207Ala
XM_024446064.1:c.575A>C XP_024301832.1:p.Glu192Ala
XR_001742071.1:n.678A>C
XR_001742072.1:n.678A>C
XR_001742074.1:n.678A>C
XR_001742075.1:n.678A>C
XR_001742076.1:n.678A>C
XR_001742077.1:n.678A>C
NM_001364440.2:c.575A>C NP_001351369.1:p.Glu192Ala
NM_001364441.2:c.575A>C NP_001351370.1:p.Glu192Ala
NM_001364442.2:c.575A>C NP_001351371.1:p.Glu192Ala
NM_002454.3:c.575A>C MANE Select NP_002445.2:p.Glu192Ala
NM_024010.4:c.575A>C NP_076915.3:p.Glu192Ala
NR_134480.2:n.654A>C
NR_134481.2:n.668A>C
NR_134482.2:n.514A>C
NR_157168.2:n.628A>C
NR_157169.2:n.488A>C
NR_157170.2:n.514A>C
NR_157171.2:n.488A>C
NR_157172.2:n.514A>C
NR_157173.2:n.642A>C
NR_157174.2:n.514A>C
NR_157175.2:n.668A>C
NR_157176.2:n.668A>C
NR_157177.2:n.663A>C
NR_157178.2:n.668A>C