Canonical Allele Identifier: CA359156697

Gene: MTRR

Linked Data

• MyVariant Identifiers: chr5:g.7878076C>A (hg19) ; chr5:g.7877963C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7877963C>A , CM000667.2:g.7877963C>A	GRCh38
NC_000005.9:g.7878076C>A , CM000667.1:g.7878076C>A	GRCh37
NC_000005.8:g.7931076C>A	NCBI36
NG_008856.1:g.13860C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440940.7:c.421C>A MANE Select	ENSP00000402510.2:p.Pro141Thr
ENST00000264668.6:c.502C>A	ENSP00000264668.2:p.Pro168Thr
ENST00000440940.6:c.421C>A	ENSP00000402510.2:p.Pro141Thr
ENST00000502509.5:n.636C>A
ENST00000502550.5:c.421C>A	ENSP00000424599.1:p.Pro141Thr
ENST00000503550.5:c.*356C>A	ENSP00000424644.1:n.*356C>A
ENST00000508047.5:c.474C>A
ENST00000508890.1:n.234C>A
ENST00000510279.5:c.*90C>A	ENSP00000427200.1:n.*90C>A
ENST00000510525.5:c.446C>A
ENST00000511461.5:c.334C>A
ENST00000513439.5:c.*128C>A	ENSP00000426710.1:n.*128C>A
ENST00000514220.5:c.206C>A
ENST00000514369.5:c.*85C>A	ENSP00000426132.1:n.*85C>A
NM_002454.2:c.421C>A	NP_002445.2:p.Pro141Thr
NM_024010.2:c.502C>A	NP_076915.2:p.Pro168Thr
XM_006714474.2:c.502C>A	XP_006714537.1:p.Pro168Thr
XM_011514043.1:c.502C>A	XP_011512345.1:p.Pro168Thr
XM_011514044.1:c.421C>A	XP_011512346.1:p.Pro141Thr
XM_011514045.1:c.502C>A	XP_011512347.1:p.Pro168Thr
XR_241702.1:n.524C>A
XR_241703.1:n.517C>A
XR_925614.1:n.524C>A
XR_925615.1:n.524C>A
NM_001364440.1:c.421C>A	NP_001351369.1:p.Pro141Thr
NM_001364441.1:c.421C>A	NP_001351370.1:p.Pro141Thr
NM_001364442.1:c.421C>A	NP_001351371.1:p.Pro141Thr
NM_024010.3:c.421C>A	NP_076915.3:p.Pro141Thr
NR_134480.1:n.544C>A
NR_134481.1:n.558C>A
NR_134482.1:n.404C>A
NR_157168.1:n.474C>A
NR_157169.1:n.334C>A
NR_157170.1:n.360C>A
NR_157171.1:n.334C>A
NR_157172.1:n.360C>A
NR_157173.1:n.488C>A
NR_157174.1:n.360C>A
NR_157175.1:n.514C>A
NR_157176.1:n.514C>A
NR_157177.1:n.509C>A
NR_157178.1:n.514C>A
XM_024446063.1:c.466C>A	XP_024301831.1:p.Pro156Thr
XM_024446064.1:c.421C>A	XP_024301832.1:p.Pro141Thr
XR_001742071.1:n.524C>A
XR_001742072.1:n.524C>A
XR_001742074.1:n.524C>A
XR_001742075.1:n.524C>A
XR_001742076.1:n.524C>A
XR_001742077.1:n.524C>A
NM_001364440.2:c.421C>A	NP_001351369.1:p.Pro141Thr
NM_001364441.2:c.421C>A	NP_001351370.1:p.Pro141Thr
NM_001364442.2:c.421C>A	NP_001351371.1:p.Pro141Thr
NM_002454.3:c.421C>A MANE Select	NP_002445.2:p.Pro141Thr
NM_024010.4:c.421C>A	NP_076915.3:p.Pro141Thr
NR_134480.2:n.500C>A
NR_134481.2:n.514C>A
NR_134482.2:n.360C>A
NR_157168.2:n.474C>A
NR_157169.2:n.334C>A
NR_157170.2:n.360C>A
NR_157171.2:n.334C>A
NR_157172.2:n.360C>A
NR_157173.2:n.488C>A
NR_157174.2:n.360C>A
NR_157175.2:n.514C>A
NR_157176.2:n.514C>A
NR_157177.2:n.509C>A
NR_157178.2:n.514C>A