Canonical Allele Identifier: CA1525815739
Gene: MTRR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.7885122A= , CM000667.2:g.7885122A= GRCh38
NC_000005.9:g.7885235A= , CM000667.1:g.7885235A= GRCh37
NC_000005.8:g.7938235A= NCBI36
NG_008856.1:g.21019A=

Transcript Alleles

HGVS Amino-acid change
ENST00000440940.7:c.904-579A= MANE Select ENSP00000402510.2:n.904-579A=
ENST00000264668.6:c.985-579A= ENSP00000264668.2:n.985-579A=
ENST00000440940.6:c.904-579A= ENSP00000402510.2:n.904-579A=
ENST00000508101.5:n.7A=
ENST00000510525.5:c.929-579A=
ENST00000511461.5:c.817-579A=
ENST00000513439.5:c.*611-579A= ENSP00000426710.1:n.*611-579A=
NM_002454.2:c.904-579A= NP_002445.2:n.904-579A=
NM_024010.2:c.985-579A= NP_076915.2:n.985-579A=
XM_006714474.2:c.985-579A= XP_006714537.1:n.985-579A=
XM_011514043.1:c.985-579A= XP_011512345.1:n.985-579A=
XM_011514044.1:c.904-579A= XP_011512346.1:n.904-579A=
XM_011514045.1:c.1125-579A= XP_011512347.1:n.1125-579A=
XR_241702.1:n.1007-579A=
XR_241703.1:n.1000-579A=
XR_925614.1:n.1007-579A=
XR_925615.1:n.1007-579A=
NM_001364440.1:c.904-579A= NP_001351369.1:n.904-579A=
NM_001364441.1:c.904-579A= NP_001351370.1:n.904-579A=
NM_001364442.1:c.904-579A= NP_001351371.1:n.904-579A=
NM_024010.3:c.904-579A= NP_076915.3:n.904-579A=
NR_134480.1:n.1027-579A=
NR_134481.1:n.1041-579A=
NR_134482.1:n.887-579A=
NR_157168.1:n.957-579A=
NR_157169.1:n.817-579A=
NR_157170.1:n.983-579A=
NR_157171.1:n.817-579A=
NR_157172.1:n.843-579A=
NR_157173.1:n.971-579A=
NR_157174.1:n.843-579A=
NR_157175.1:n.997-579A=
NR_157176.1:n.1137-579A=
NR_157177.1:n.992-579A=
NR_157178.1:n.997-579A=
XM_024446063.1:c.949-579A= XP_024301831.1:n.949-579A=
XM_024446064.1:c.904-579A= XP_024301832.1:n.904-579A=
XR_001742071.1:n.1007-579A=
XR_001742072.1:n.1007-579A=
XR_001742074.1:n.1007-579A=
XR_001742075.1:n.1007-579A=
XR_001742076.1:n.1147-579A=
XR_001742077.1:n.1147-579A=
NM_001364440.2:c.904-579A= NP_001351369.1:n.904-579A=
NM_001364441.2:c.904-579A= NP_001351370.1:n.904-579A=
NM_001364442.2:c.904-579A= NP_001351371.1:n.904-579A=
NM_002454.3:c.904-579A= MANE Select NP_002445.2:n.904-579A=
NM_024010.4:c.904-579A= NP_076915.3:n.904-579A=
NR_134480.2:n.983-579A=
NR_134481.2:n.997-579A=
NR_134482.2:n.843-579A=
NR_157168.2:n.957-579A=
NR_157169.2:n.817-579A=
NR_157170.2:n.983-579A=
NR_157171.2:n.817-579A=
NR_157172.2:n.843-579A=
NR_157173.2:n.971-579A=
NR_157174.2:n.843-579A=
NR_157175.2:n.997-579A=
NR_157176.2:n.1137-579A=
NR_157177.2:n.992-579A=
NR_157178.2:n.997-579A=