Canonical Allele Identifier: CA2673202912

Gene: MTRR

Linked Data

• gnomAD v4: 5-7891317-AAGGTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7891319_7891323del , CM000667.2:g.7891319_7891323del	GRCh38
NC_000005.9:g.7891432_7891436del , CM000667.1:g.7891432_7891436del	GRCh37
NC_000005.8:g.7944432_7944436del	NCBI36
NG_008856.1:g.27216_27220del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440940.7:c.1328-53_1328-49del MANE Select	ENSP00000402510.2:n.1328-53_1328-49del
ENST00000264668.6:c.1409-53_1409-49del	ENSP00000264668.2:n.1409-53_1409-49del
ENST00000440940.6:c.1328-53_1328-49del	ENSP00000402510.2:n.1328-53_1328-49del
ENST00000507414.1:n.68-53_68-49del
ENST00000508101.5:n.568-53_568-49del
ENST00000510525.5:c.1264-53_1264-49del
ENST00000511461.5:c.1241-53_1241-49del
ENST00000512311.5:n.307-53_307-49del
ENST00000513439.5:c.*1035-53_*1035-49del	ENSP00000426710.1:n.*1035-53_*1035-49del
NM_002454.2:c.1328-53_1328-49del	NP_002445.2:n.1328-53_1328-49del
NM_024010.2:c.1409-53_1409-49del	NP_076915.2:n.1409-53_1409-49del
XM_011514043.1:c.1409-53_1409-49del	XP_011512345.1:n.1409-53_1409-49del
XM_011514044.1:c.1328-53_1328-49del	XP_011512346.1:n.1328-53_1328-49del
XR_241702.1:n.1342-53_1342-49del
XR_241703.1:n.1335-53_1335-49del
XR_925614.1:n.1454-53_1454-49del
XR_925615.1:n.1606-53_1606-49del
NM_001364440.1:c.1328-53_1328-49del	NP_001351369.1:n.1328-53_1328-49del
NM_001364441.1:c.1328-53_1328-49del	NP_001351370.1:n.1328-53_1328-49del
NM_001364442.1:c.1328-53_1328-49del	NP_001351371.1:n.1328-53_1328-49del
NM_024010.3:c.1328-53_1328-49del	NP_076915.3:n.1328-53_1328-49del
NR_134480.1:n.1451-53_1451-49del
NR_134481.1:n.1376-53_1376-49del
NR_134482.1:n.1311-53_1311-49del
NR_157168.1:n.1381-53_1381-49del
NR_157169.1:n.1241-53_1241-49del
NR_157170.1:n.1407-53_1407-49del
NR_157171.1:n.1264-53_1264-49del
NR_157172.1:n.1178-53_1178-49del
NR_157173.1:n.1418-53_1418-49del
NR_157174.1:n.1419-53_1419-49del
NR_157175.1:n.1573-53_1573-49del
NR_157176.1:n.1736-53_1736-49del
NR_157177.1:n.1416-53_1416-49del
NR_157178.1:n.1444-53_1444-49del
XM_024446063.1:c.1373-53_1373-49del	XP_024301831.1:n.1373-53_1373-49del
XM_024446064.1:c.1328-53_1328-49del	XP_024301832.1:n.1328-53_1328-49del
XR_001742071.1:n.1606-53_1606-49del
XR_001742072.1:n.1583-53_1583-49del
XR_001742074.1:n.1342-53_1342-49del
XR_001742075.1:n.1494-53_1494-49del
XR_001742076.1:n.1571-53_1571-49del
XR_001742077.1:n.1594-53_1594-49del
NM_001364440.2:c.1328-53_1328-49del	NP_001351369.1:n.1328-53_1328-49del
NM_001364441.2:c.1328-53_1328-49del	NP_001351370.1:n.1328-53_1328-49del
NM_001364442.2:c.1328-53_1328-49del	NP_001351371.1:n.1328-53_1328-49del
NM_002454.3:c.1328-53_1328-49del MANE Select	NP_002445.2:n.1328-53_1328-49del
NM_024010.4:c.1328-53_1328-49del	NP_076915.3:n.1328-53_1328-49del
NR_134480.2:n.1407-53_1407-49del
NR_134481.2:n.1332-53_1332-49del
NR_134482.2:n.1267-53_1267-49del
NR_157168.2:n.1381-53_1381-49del
NR_157169.2:n.1241-53_1241-49del
NR_157170.2:n.1407-53_1407-49del
NR_157171.2:n.1264-53_1264-49del
NR_157172.2:n.1178-53_1178-49del
NR_157173.2:n.1418-53_1418-49del
NR_157174.2:n.1419-53_1419-49del
NR_157175.2:n.1573-53_1573-49del
NR_157176.2:n.1736-53_1736-49del
NR_157177.2:n.1416-53_1416-49del
NR_157178.2:n.1444-53_1444-49del