Canonical Allele Identifier: CA2673201495

Gene: MTRR

Linked Data

• gnomAD v4: 5-7885136-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7885138del , CM000667.2:g.7885138del	GRCh38
NC_000005.9:g.7885251del , CM000667.1:g.7885251del	GRCh37
NC_000005.8:g.7938251del	NCBI36
NG_008856.1:g.21035del

Transcript Alleles

HGVS	Amino-acid change
ENST00000440940.7:c.904-563del MANE Select	ENSP00000402510.2:n.904-563del
ENST00000264668.6:c.985-563del	ENSP00000264668.2:n.985-563del
ENST00000440940.6:c.904-563del	ENSP00000402510.2:n.904-563del
ENST00000508101.5:n.23del
ENST00000510525.5:c.929-563del
ENST00000511461.5:c.817-563del
ENST00000513439.5:c.*611-563del	ENSP00000426710.1:n.*611-563del
NM_002454.2:c.904-563del	NP_002445.2:n.904-563del
NM_024010.2:c.985-563del	NP_076915.2:n.985-563del
XM_006714474.2:c.985-563del	XP_006714537.1:n.985-563del
XM_011514043.1:c.985-563del	XP_011512345.1:n.985-563del
XM_011514044.1:c.904-563del	XP_011512346.1:n.904-563del
XM_011514045.1:c.1125-563del	XP_011512347.1:n.1125-563del
XR_241702.1:n.1007-563del
XR_241703.1:n.1000-563del
XR_925614.1:n.1007-563del
XR_925615.1:n.1007-563del
NM_001364440.1:c.904-563del	NP_001351369.1:n.904-563del
NM_001364441.1:c.904-563del	NP_001351370.1:n.904-563del
NM_001364442.1:c.904-563del	NP_001351371.1:n.904-563del
NM_024010.3:c.904-563del	NP_076915.3:n.904-563del
NR_134480.1:n.1027-563del
NR_134481.1:n.1041-563del
NR_134482.1:n.887-563del
NR_157168.1:n.957-563del
NR_157169.1:n.817-563del
NR_157170.1:n.983-563del
NR_157171.1:n.817-563del
NR_157172.1:n.843-563del
NR_157173.1:n.971-563del
NR_157174.1:n.843-563del
NR_157175.1:n.997-563del
NR_157176.1:n.1137-563del
NR_157177.1:n.992-563del
NR_157178.1:n.997-563del
XM_024446063.1:c.949-563del	XP_024301831.1:n.949-563del
XM_024446064.1:c.904-563del	XP_024301832.1:n.904-563del
XR_001742071.1:n.1007-563del
XR_001742072.1:n.1007-563del
XR_001742074.1:n.1007-563del
XR_001742075.1:n.1007-563del
XR_001742076.1:n.1147-563del
XR_001742077.1:n.1147-563del
NM_001364440.2:c.904-563del	NP_001351369.1:n.904-563del
NM_001364441.2:c.904-563del	NP_001351370.1:n.904-563del
NM_001364442.2:c.904-563del	NP_001351371.1:n.904-563del
NM_002454.3:c.904-563del MANE Select	NP_002445.2:n.904-563del
NM_024010.4:c.904-563del	NP_076915.3:n.904-563del
NR_134480.2:n.983-563del
NR_134481.2:n.997-563del
NR_134482.2:n.843-563del
NR_157168.2:n.957-563del
NR_157169.2:n.817-563del
NR_157170.2:n.983-563del
NR_157171.2:n.817-563del
NR_157172.2:n.843-563del
NR_157173.2:n.971-563del
NR_157174.2:n.843-563del
NR_157175.2:n.997-563del
NR_157176.2:n.1137-563del
NR_157177.2:n.992-563del
NR_157178.2:n.997-563del