Canonical Allele Identifier: CA2673201623

Gene: MTRR

Linked Data

• gnomAD v4: 5-7885330-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7885330_7885331insT , CM000667.2:g.7885330_7885331insT	GRCh38
NC_000005.9:g.7885443_7885444insT , CM000667.1:g.7885443_7885444insT	GRCh37
NC_000005.8:g.7938443_7938444insT	NCBI36
NG_008856.1:g.21227_21228insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440940.7:c.904-371_904-370insT MANE Select	ENSP00000402510.2:n.904-371_904-370insT
ENST00000264668.6:c.985-371_985-370insT	ENSP00000264668.2:n.985-371_985-370insT
ENST00000440940.6:c.904-371_904-370insT	ENSP00000402510.2:n.904-371_904-370insT
ENST00000508101.5:n.143+72_143+73insT
ENST00000510525.5:c.929-371_929-370insT
ENST00000511461.5:c.817-371_817-370insT
ENST00000513439.5:c.*611-371_*611-370insT	ENSP00000426710.1:n.*611-371_*611-370insT
NM_002454.2:c.904-371_904-370insT	NP_002445.2:n.904-371_904-370insT
NM_024010.2:c.985-371_985-370insT	NP_076915.2:n.985-371_985-370insT
XM_006714474.2:c.985-371_985-370insT	XP_006714537.1:n.985-371_985-370insT
XM_011514043.1:c.985-371_985-370insT	XP_011512345.1:n.985-371_985-370insT
XM_011514044.1:c.904-371_904-370insT	XP_011512346.1:n.904-371_904-370insT
XM_011514045.1:c.1125-371_1125-370insT	XP_011512347.1:n.1125-371_1125-370insT
XR_241702.1:n.1007-371_1007-370insT
XR_241703.1:n.1000-371_1000-370insT
XR_925614.1:n.1007-371_1007-370insT
XR_925615.1:n.1007-371_1007-370insT
NM_001364440.1:c.904-371_904-370insT	NP_001351369.1:n.904-371_904-370insT
NM_001364441.1:c.904-371_904-370insT	NP_001351370.1:n.904-371_904-370insT
NM_001364442.1:c.904-371_904-370insT	NP_001351371.1:n.904-371_904-370insT
NM_024010.3:c.904-371_904-370insT	NP_076915.3:n.904-371_904-370insT
NR_134480.1:n.1027-371_1027-370insT
NR_134481.1:n.1041-371_1041-370insT
NR_134482.1:n.887-371_887-370insT
NR_157168.1:n.957-371_957-370insT
NR_157169.1:n.817-371_817-370insT
NR_157170.1:n.983-371_983-370insT
NR_157171.1:n.817-371_817-370insT
NR_157172.1:n.843-371_843-370insT
NR_157173.1:n.971-371_971-370insT
NR_157174.1:n.843-371_843-370insT
NR_157175.1:n.997-371_997-370insT
NR_157176.1:n.1137-371_1137-370insT
NR_157177.1:n.992-371_992-370insT
NR_157178.1:n.997-371_997-370insT
XM_024446063.1:c.949-371_949-370insT	XP_024301831.1:n.949-371_949-370insT
XM_024446064.1:c.904-371_904-370insT	XP_024301832.1:n.904-371_904-370insT
XR_001742071.1:n.1007-371_1007-370insT
XR_001742072.1:n.1007-371_1007-370insT
XR_001742074.1:n.1007-371_1007-370insT
XR_001742075.1:n.1007-371_1007-370insT
XR_001742076.1:n.1147-371_1147-370insT
XR_001742077.1:n.1147-371_1147-370insT
NM_001364440.2:c.904-371_904-370insT	NP_001351369.1:n.904-371_904-370insT
NM_001364441.2:c.904-371_904-370insT	NP_001351370.1:n.904-371_904-370insT
NM_001364442.2:c.904-371_904-370insT	NP_001351371.1:n.904-371_904-370insT
NM_002454.3:c.904-371_904-370insT MANE Select	NP_002445.2:n.904-371_904-370insT
NM_024010.4:c.904-371_904-370insT	NP_076915.3:n.904-371_904-370insT
NR_134480.2:n.983-371_983-370insT
NR_134481.2:n.997-371_997-370insT
NR_134482.2:n.843-371_843-370insT
NR_157168.2:n.957-371_957-370insT
NR_157169.2:n.817-371_817-370insT
NR_157170.2:n.983-371_983-370insT
NR_157171.2:n.817-371_817-370insT
NR_157172.2:n.843-371_843-370insT
NR_157173.2:n.971-371_971-370insT
NR_157174.2:n.843-371_843-370insT
NR_157175.2:n.997-371_997-370insT
NR_157176.2:n.1137-371_1137-370insT
NR_157177.2:n.992-371_992-370insT
NR_157178.2:n.997-371_997-370insT