Canonical Allele Identifier: CA1072984150
Gene: MTRR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.7891327_7891328insTTTTTT , CM000667.2:g.7891327_7891328insTTTTTT GRCh38
NC_000005.9:g.7891440_7891441insTTTTTT , CM000667.1:g.7891440_7891441insTTTTTT GRCh37
NC_000005.8:g.7944440_7944441insTTTTTT NCBI36
NG_008856.1:g.27224_27225insTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000440940.7:c.1328-45_1328-44insTTTTTT MANE Select ENSP00000402510.2:n.1328-45_1328-44insTTTTTT
ENST00000264668.6:c.1409-45_1409-44insTTTTTT ENSP00000264668.2:n.1409-45_1409-44insTTTTTT
ENST00000440940.6:c.1328-45_1328-44insTTTTTT ENSP00000402510.2:n.1328-45_1328-44insTTTTTT
ENST00000507414.1:n.68-45_68-44insTTTTTT
ENST00000508101.5:n.568-45_568-44insTTTTTT
ENST00000510525.5:c.1264-45_1264-44insTTTTTT
ENST00000511461.5:c.1241-45_1241-44insTTTTTT
ENST00000512311.5:n.307-45_307-44insTTTTTT
ENST00000513439.5:c.*1035-45_*1035-44insTTTTTT ENSP00000426710.1:n.*1035-45_*1035-44insTTTTTT
NM_002454.2:c.1328-45_1328-44insTTTTTT NP_002445.2:n.1328-45_1328-44insTTTTTT
NM_024010.2:c.1409-45_1409-44insTTTTTT NP_076915.2:n.1409-45_1409-44insTTTTTT
XM_011514043.1:c.1409-45_1409-44insTTTTTT XP_011512345.1:n.1409-45_1409-44insTTTTTT
XM_011514044.1:c.1328-45_1328-44insTTTTTT XP_011512346.1:n.1328-45_1328-44insTTTTTT
XR_241702.1:n.1342-45_1342-44insTTTTTT
XR_241703.1:n.1335-45_1335-44insTTTTTT
XR_925614.1:n.1454-45_1454-44insTTTTTT
XR_925615.1:n.1606-45_1606-44insTTTTTT
NM_001364440.1:c.1328-45_1328-44insTTTTTT NP_001351369.1:n.1328-45_1328-44insTTTTTT
NM_001364441.1:c.1328-45_1328-44insTTTTTT NP_001351370.1:n.1328-45_1328-44insTTTTTT
NM_001364442.1:c.1328-45_1328-44insTTTTTT NP_001351371.1:n.1328-45_1328-44insTTTTTT
NM_024010.3:c.1328-45_1328-44insTTTTTT NP_076915.3:n.1328-45_1328-44insTTTTTT
NR_134480.1:n.1451-45_1451-44insTTTTTT
NR_134481.1:n.1376-45_1376-44insTTTTTT
NR_134482.1:n.1311-45_1311-44insTTTTTT
NR_157168.1:n.1381-45_1381-44insTTTTTT
NR_157169.1:n.1241-45_1241-44insTTTTTT
NR_157170.1:n.1407-45_1407-44insTTTTTT
NR_157171.1:n.1264-45_1264-44insTTTTTT
NR_157172.1:n.1178-45_1178-44insTTTTTT
NR_157173.1:n.1418-45_1418-44insTTTTTT
NR_157174.1:n.1419-45_1419-44insTTTTTT
NR_157175.1:n.1573-45_1573-44insTTTTTT
NR_157176.1:n.1736-45_1736-44insTTTTTT
NR_157177.1:n.1416-45_1416-44insTTTTTT
NR_157178.1:n.1444-45_1444-44insTTTTTT
XM_024446063.1:c.1373-45_1373-44insTTTTTT XP_024301831.1:n.1373-45_1373-44insTTTTTT
XM_024446064.1:c.1328-45_1328-44insTTTTTT XP_024301832.1:n.1328-45_1328-44insTTTTTT
XR_001742071.1:n.1606-45_1606-44insTTTTTT
XR_001742072.1:n.1583-45_1583-44insTTTTTT
XR_001742074.1:n.1342-45_1342-44insTTTTTT
XR_001742075.1:n.1494-45_1494-44insTTTTTT
XR_001742076.1:n.1571-45_1571-44insTTTTTT
XR_001742077.1:n.1594-45_1594-44insTTTTTT
NM_001364440.2:c.1328-45_1328-44insTTTTTT NP_001351369.1:n.1328-45_1328-44insTTTTTT
NM_001364441.2:c.1328-45_1328-44insTTTTTT NP_001351370.1:n.1328-45_1328-44insTTTTTT
NM_001364442.2:c.1328-45_1328-44insTTTTTT NP_001351371.1:n.1328-45_1328-44insTTTTTT
NM_002454.3:c.1328-45_1328-44insTTTTTT MANE Select NP_002445.2:n.1328-45_1328-44insTTTTTT
NM_024010.4:c.1328-45_1328-44insTTTTTT NP_076915.3:n.1328-45_1328-44insTTTTTT
NR_134480.2:n.1407-45_1407-44insTTTTTT
NR_134481.2:n.1332-45_1332-44insTTTTTT
NR_134482.2:n.1267-45_1267-44insTTTTTT
NR_157168.2:n.1381-45_1381-44insTTTTTT
NR_157169.2:n.1241-45_1241-44insTTTTTT
NR_157170.2:n.1407-45_1407-44insTTTTTT
NR_157171.2:n.1264-45_1264-44insTTTTTT
NR_157172.2:n.1178-45_1178-44insTTTTTT
NR_157173.2:n.1418-45_1418-44insTTTTTT
NR_157174.2:n.1419-45_1419-44insTTTTTT
NR_157175.2:n.1573-45_1573-44insTTTTTT
NR_157176.2:n.1736-45_1736-44insTTTTTT
NR_157177.2:n.1416-45_1416-44insTTTTTT
NR_157178.2:n.1444-45_1444-44insTTTTTT