Canonical Allele Identifier: CA2673203622
Gene: MTRR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.7895756_7895758del , CM000667.2:g.7895756_7895758del GRCh38
NC_000005.9:g.7895869_7895871del , CM000667.1:g.7895869_7895871del GRCh37
NC_000005.8:g.7948869_7948871del NCBI36
NG_008856.1:g.31653_31655del

Transcript Alleles

HGVS Amino-acid change
ENST00000440940.7:c.1580_1582del MANE Select ENSP00000402510.2:p.Thr527del
ENST00000264668.6:c.1661_1663del ENSP00000264668.2:p.Thr554del
ENST00000440940.6:c.1580_1582del ENSP00000402510.2:p.Thr527del
ENST00000510525.5:c.1516_1518del
ENST00000511461.5:c.1493_1495del
ENST00000513439.5:c.*1287_*1289del ENSP00000426710.1:n.*1287_*1289del
NM_002454.2:c.1580_1582del NP_002445.2:p.Thr527del
NM_024010.2:c.1661_1663del NP_076915.2:p.Thr554del
XM_011514043.1:c.1661_1663del XP_011512345.1:p.Thr554del
XM_011514044.1:c.1580_1582del XP_011512346.1:p.Thr527del
XR_241702.1:n.1594_1596del
XR_241703.1:n.1587_1589del
XR_925614.1:n.1706_1708del
NM_001364440.1:c.1580_1582del NP_001351369.1:p.Thr527del
NM_001364441.1:c.1580_1582del NP_001351370.1:p.Thr527del
NM_001364442.1:c.1580_1582del NP_001351371.1:p.Thr527del
NM_024010.3:c.1580_1582del NP_076915.3:p.Thr527del
NR_134480.1:n.1703_1705del
NR_134481.1:n.1628_1630del
NR_134482.1:n.1563_1565del
NR_157168.1:n.1633_1635del
NR_157169.1:n.1493_1495del
NR_157170.1:n.1659_1661del
NR_157171.1:n.1516_1518del
NR_157172.1:n.1430_1432del
NR_157173.1:n.1670_1672del
NR_157174.1:n.1671_1673del
NR_157175.1:n.1825_1827del
NR_157176.1:n.1988_1990del
NR_157177.1:n.1668_1670del
NR_157178.1:n.1696_1698del
XM_024446063.1:c.1625_1627del XP_024301831.1:p.Thr542del
XM_024446064.1:c.1580_1582del XP_024301832.1:p.Thr527del
XR_001742071.1:n.1858_1860del
XR_001742072.1:n.1835_1837del
XR_001742074.1:n.1594_1596del
XR_001742075.1:n.1746_1748del
XR_001742076.1:n.1823_1825del
XR_001742077.1:n.1846_1848del
NM_001364440.2:c.1580_1582del NP_001351369.1:p.Thr527del
NM_001364441.2:c.1580_1582del NP_001351370.1:p.Thr527del
NM_001364442.2:c.1580_1582del NP_001351371.1:p.Thr527del
NM_002454.3:c.1580_1582del MANE Select NP_002445.2:p.Thr527del
NM_024010.4:c.1580_1582del NP_076915.3:p.Thr527del
NR_134480.2:n.1659_1661del
NR_134481.2:n.1584_1586del
NR_134482.2:n.1519_1521del
NR_157168.2:n.1633_1635del
NR_157169.2:n.1493_1495del
NR_157170.2:n.1659_1661del
NR_157171.2:n.1516_1518del
NR_157172.2:n.1430_1432del
NR_157173.2:n.1670_1672del
NR_157174.2:n.1671_1673del
NR_157175.2:n.1825_1827del
NR_157176.2:n.1988_1990del
NR_157177.2:n.1668_1670del
NR_157178.2:n.1696_1698del