Canonical Allele Identifier: CA359156680

Gene: MTRR

Linked Data

• MyVariant Identifiers: chr5:g.7878068T>A (hg19) ; chr5:g.7877955T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7877955T>A , CM000667.2:g.7877955T>A	GRCh38
NC_000005.9:g.7878068T>A , CM000667.1:g.7878068T>A	GRCh37
NC_000005.8:g.7931068T>A	NCBI36
NG_008856.1:g.13852T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440940.7:c.413T>A MANE Select	ENSP00000402510.2:p.Val138Glu
ENST00000264668.6:c.494T>A	ENSP00000264668.2:p.Val165Glu
ENST00000440940.6:c.413T>A	ENSP00000402510.2:p.Val138Glu
ENST00000502509.5:n.628T>A
ENST00000502550.5:c.413T>A	ENSP00000424599.1:p.Val138Glu
ENST00000503550.5:c.*348T>A	ENSP00000424644.1:n.*348T>A
ENST00000508047.5:c.466T>A
ENST00000508890.1:n.226T>A
ENST00000510279.5:c.*82T>A	ENSP00000427200.1:n.*82T>A
ENST00000510525.5:c.438T>A
ENST00000511461.5:c.326T>A
ENST00000513439.5:c.*120T>A	ENSP00000426710.1:n.*120T>A
ENST00000514220.5:c.198T>A
ENST00000514369.5:c.*77T>A	ENSP00000426132.1:n.*77T>A
NM_002454.2:c.413T>A	NP_002445.2:p.Val138Glu
NM_024010.2:c.494T>A	NP_076915.2:p.Val165Glu
XM_006714474.2:c.494T>A	XP_006714537.1:p.Val165Glu
XM_011514043.1:c.494T>A	XP_011512345.1:p.Val165Glu
XM_011514044.1:c.413T>A	XP_011512346.1:p.Val138Glu
XM_011514045.1:c.494T>A	XP_011512347.1:p.Val165Glu
XR_241702.1:n.516T>A
XR_241703.1:n.509T>A
XR_925614.1:n.516T>A
XR_925615.1:n.516T>A
NM_001364440.1:c.413T>A	NP_001351369.1:p.Val138Glu
NM_001364441.1:c.413T>A	NP_001351370.1:p.Val138Glu
NM_001364442.1:c.413T>A	NP_001351371.1:p.Val138Glu
NM_024010.3:c.413T>A	NP_076915.3:p.Val138Glu
NR_134480.1:n.536T>A
NR_134481.1:n.550T>A
NR_134482.1:n.396T>A
NR_157168.1:n.466T>A
NR_157169.1:n.326T>A
NR_157170.1:n.352T>A
NR_157171.1:n.326T>A
NR_157172.1:n.352T>A
NR_157173.1:n.480T>A
NR_157174.1:n.352T>A
NR_157175.1:n.506T>A
NR_157176.1:n.506T>A
NR_157177.1:n.501T>A
NR_157178.1:n.506T>A
XM_024446063.1:c.458T>A	XP_024301831.1:p.Val153Glu
XM_024446064.1:c.413T>A	XP_024301832.1:p.Val138Glu
XR_001742071.1:n.516T>A
XR_001742072.1:n.516T>A
XR_001742074.1:n.516T>A
XR_001742075.1:n.516T>A
XR_001742076.1:n.516T>A
XR_001742077.1:n.516T>A
NM_001364440.2:c.413T>A	NP_001351369.1:p.Val138Glu
NM_001364441.2:c.413T>A	NP_001351370.1:p.Val138Glu
NM_001364442.2:c.413T>A	NP_001351371.1:p.Val138Glu
NM_002454.3:c.413T>A MANE Select	NP_002445.2:p.Val138Glu
NM_024010.4:c.413T>A	NP_076915.3:p.Val138Glu
NR_134480.2:n.492T>A
NR_134481.2:n.506T>A
NR_134482.2:n.352T>A
NR_157168.2:n.466T>A
NR_157169.2:n.326T>A
NR_157170.2:n.352T>A
NR_157171.2:n.326T>A
NR_157172.2:n.352T>A
NR_157173.2:n.480T>A
NR_157174.2:n.352T>A
NR_157175.2:n.506T>A
NR_157176.2:n.506T>A
NR_157177.2:n.501T>A
NR_157178.2:n.506T>A