Canonical Allele Identifier: CA2673201939

Gene: MTRR

Linked Data

• gnomAD v4: 5-7877813-TCCGAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7877814_7877818del , CM000667.2:g.7877814_7877818del	GRCh38
NC_000005.9:g.7877927_7877931del , CM000667.1:g.7877927_7877931del	GRCh37
NC_000005.8:g.7930927_7930931del	NCBI36
NG_008856.1:g.13711_13715del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440940.7:c.402-130_402-126del MANE Select	ENSP00000402510.2:n.402-130_402-126del
ENST00000264668.6:c.483-130_483-126del	ENSP00000264668.2:n.483-130_483-126del
ENST00000440940.6:c.402-130_402-126del	ENSP00000402510.2:n.402-130_402-126del
ENST00000502509.5:n.617-130_617-126del
ENST00000502550.5:c.402-130_402-126del	ENSP00000424599.1:n.402-130_402-126del
ENST00000503550.5:c.*337-130_*337-126del	ENSP00000424644.1:n.*337-130_*337-126del
ENST00000508047.5:c.455-130_455-126del
ENST00000508890.1:n.215-130_215-126del
ENST00000510279.5:c.*71-130_*71-126del	ENSP00000427200.1:n.*71-130_*71-126del
ENST00000510525.5:c.427-130_427-126del
ENST00000511461.5:c.315-130_315-126del
ENST00000513439.5:c.*109-130_*109-126del	ENSP00000426710.1:n.*109-130_*109-126del
ENST00000514220.5:c.187-130_187-126del
ENST00000514369.5:c.*71-135_*71-131del	ENSP00000426132.1:n.*71-135_*71-131del
NM_002454.2:c.402-130_402-126del	NP_002445.2:n.402-130_402-126del
NM_024010.2:c.483-130_483-126del	NP_076915.2:n.483-130_483-126del
XM_006714474.2:c.483-130_483-126del	XP_006714537.1:n.483-130_483-126del
XM_011514043.1:c.483-130_483-126del	XP_011512345.1:n.483-130_483-126del
XM_011514044.1:c.402-130_402-126del	XP_011512346.1:n.402-130_402-126del
XM_011514045.1:c.483-130_483-126del	XP_011512347.1:n.483-130_483-126del
XR_241702.1:n.505-130_505-126del
XR_241703.1:n.498-130_498-126del
XR_925614.1:n.505-130_505-126del
XR_925615.1:n.505-130_505-126del
NM_001364440.1:c.402-130_402-126del	NP_001351369.1:n.402-130_402-126del
NM_001364441.1:c.402-130_402-126del	NP_001351370.1:n.402-130_402-126del
NM_001364442.1:c.402-130_402-126del	NP_001351371.1:n.402-130_402-126del
NM_024010.3:c.402-130_402-126del	NP_076915.3:n.402-130_402-126del
NR_134480.1:n.525-130_525-126del
NR_134481.1:n.539-130_539-126del
NR_134482.1:n.385-130_385-126del
NR_157168.1:n.455-130_455-126del
NR_157169.1:n.315-130_315-126del
NR_157170.1:n.341-130_341-126del
NR_157171.1:n.315-130_315-126del
NR_157172.1:n.341-130_341-126del
NR_157173.1:n.469-130_469-126del
NR_157174.1:n.341-130_341-126del
NR_157175.1:n.495-130_495-126del
NR_157176.1:n.495-130_495-126del
NR_157177.1:n.495-135_495-131del
NR_157178.1:n.495-130_495-126del
XM_024446063.1:c.447-130_447-126del	XP_024301831.1:n.447-130_447-126del
XM_024446064.1:c.402-130_402-126del	XP_024301832.1:n.402-130_402-126del
XR_001742071.1:n.505-130_505-126del
XR_001742072.1:n.505-130_505-126del
XR_001742074.1:n.505-130_505-126del
XR_001742075.1:n.505-130_505-126del
XR_001742076.1:n.505-130_505-126del
XR_001742077.1:n.505-130_505-126del
NM_001364440.2:c.402-130_402-126del	NP_001351369.1:n.402-130_402-126del
NM_001364441.2:c.402-130_402-126del	NP_001351370.1:n.402-130_402-126del
NM_001364442.2:c.402-130_402-126del	NP_001351371.1:n.402-130_402-126del
NM_002454.3:c.402-130_402-126del MANE Select	NP_002445.2:n.402-130_402-126del
NM_024010.4:c.402-130_402-126del	NP_076915.3:n.402-130_402-126del
NR_134480.2:n.481-130_481-126del
NR_134481.2:n.495-130_495-126del
NR_134482.2:n.341-130_341-126del
NR_157168.2:n.455-130_455-126del
NR_157169.2:n.315-130_315-126del
NR_157170.2:n.341-130_341-126del
NR_157171.2:n.315-130_315-126del
NR_157172.2:n.341-130_341-126del
NR_157173.2:n.469-130_469-126del
NR_157174.2:n.341-130_341-126del
NR_157175.2:n.495-130_495-126del
NR_157176.2:n.495-130_495-126del
NR_157177.2:n.495-135_495-131del
NR_157178.2:n.495-130_495-126del