Canonical Allele Identifier: CA2578265969

Gene: MTRR

Linked Data

• gnomAD v4: 5-7891309-TTTTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7891310_7891313del , CM000667.2:g.7891310_7891313del	GRCh38
NC_000005.9:g.7891423_7891426del , CM000667.1:g.7891423_7891426del	GRCh37
NC_000005.8:g.7944423_7944426del	NCBI36
NG_008856.1:g.27207_27210del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440940.7:c.1328-62_1328-59del MANE Select	ENSP00000402510.2:n.1328-62_1328-59del
ENST00000264668.6:c.1409-62_1409-59del	ENSP00000264668.2:n.1409-62_1409-59del
ENST00000440940.6:c.1328-62_1328-59del	ENSP00000402510.2:n.1328-62_1328-59del
ENST00000507414.1:n.68-62_68-59del
ENST00000508101.5:n.568-62_568-59del
ENST00000510525.5:c.1264-62_1264-59del
ENST00000511461.5:c.1241-62_1241-59del
ENST00000512311.5:n.307-62_307-59del
ENST00000513439.5:c.*1035-62_*1035-59del	ENSP00000426710.1:n.*1035-62_*1035-59del
NM_002454.2:c.1328-62_1328-59del	NP_002445.2:n.1328-62_1328-59del
NM_024010.2:c.1409-62_1409-59del	NP_076915.2:n.1409-62_1409-59del
XM_011514043.1:c.1409-62_1409-59del	XP_011512345.1:n.1409-62_1409-59del
XM_011514044.1:c.1328-62_1328-59del	XP_011512346.1:n.1328-62_1328-59del
XR_241702.1:n.1342-62_1342-59del
XR_241703.1:n.1335-62_1335-59del
XR_925614.1:n.1454-62_1454-59del
XR_925615.1:n.1606-62_1606-59del
NM_001364440.1:c.1328-62_1328-59del	NP_001351369.1:n.1328-62_1328-59del
NM_001364441.1:c.1328-62_1328-59del	NP_001351370.1:n.1328-62_1328-59del
NM_001364442.1:c.1328-62_1328-59del	NP_001351371.1:n.1328-62_1328-59del
NM_024010.3:c.1328-62_1328-59del	NP_076915.3:n.1328-62_1328-59del
NR_134480.1:n.1451-62_1451-59del
NR_134481.1:n.1376-62_1376-59del
NR_134482.1:n.1311-62_1311-59del
NR_157168.1:n.1381-62_1381-59del
NR_157169.1:n.1241-62_1241-59del
NR_157170.1:n.1407-62_1407-59del
NR_157171.1:n.1264-62_1264-59del
NR_157172.1:n.1178-62_1178-59del
NR_157173.1:n.1418-62_1418-59del
NR_157174.1:n.1419-62_1419-59del
NR_157175.1:n.1573-62_1573-59del
NR_157176.1:n.1736-62_1736-59del
NR_157177.1:n.1416-62_1416-59del
NR_157178.1:n.1444-62_1444-59del
XM_024446063.1:c.1373-62_1373-59del	XP_024301831.1:n.1373-62_1373-59del
XM_024446064.1:c.1328-62_1328-59del	XP_024301832.1:n.1328-62_1328-59del
XR_001742071.1:n.1606-62_1606-59del
XR_001742072.1:n.1583-62_1583-59del
XR_001742074.1:n.1342-62_1342-59del
XR_001742075.1:n.1494-62_1494-59del
XR_001742076.1:n.1571-62_1571-59del
XR_001742077.1:n.1594-62_1594-59del
NM_001364440.2:c.1328-62_1328-59del	NP_001351369.1:n.1328-62_1328-59del
NM_001364441.2:c.1328-62_1328-59del	NP_001351370.1:n.1328-62_1328-59del
NM_001364442.2:c.1328-62_1328-59del	NP_001351371.1:n.1328-62_1328-59del
NM_002454.3:c.1328-62_1328-59del MANE Select	NP_002445.2:n.1328-62_1328-59del
NM_024010.4:c.1328-62_1328-59del	NP_076915.3:n.1328-62_1328-59del
NR_134480.2:n.1407-62_1407-59del
NR_134481.2:n.1332-62_1332-59del
NR_134482.2:n.1267-62_1267-59del
NR_157168.2:n.1381-62_1381-59del
NR_157169.2:n.1241-62_1241-59del
NR_157170.2:n.1407-62_1407-59del
NR_157171.2:n.1264-62_1264-59del
NR_157172.2:n.1178-62_1178-59del
NR_157173.2:n.1418-62_1418-59del
NR_157174.2:n.1419-62_1419-59del
NR_157175.2:n.1573-62_1573-59del
NR_157176.2:n.1736-62_1736-59del
NR_157177.2:n.1416-62_1416-59del
NR_157178.2:n.1444-62_1444-59del