Canonical Allele Identifier: CA359157758
Gene: MTRR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.7885711T>C , CM000667.2:g.7885711T>C GRCh38
NC_000005.9:g.7885824T>C , CM000667.1:g.7885824T>C GRCh37
NC_000005.8:g.7938824T>C NCBI36
NG_008856.1:g.21608T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000440940.7:c.914T>C MANE Select ENSP00000402510.2:p.Phe305Ser
ENST00000264668.6:c.995T>C ENSP00000264668.2:p.Phe332Ser
ENST00000440940.6:c.914T>C ENSP00000402510.2:p.Phe305Ser
ENST00000508101.5:n.154T>C
ENST00000510525.5:c.939T>C
ENST00000511461.5:c.827T>C
ENST00000513439.5:c.*621T>C ENSP00000426710.1:n.*621T>C
NM_002454.2:c.914T>C NP_002445.2:p.Phe305Ser
NM_024010.2:c.995T>C NP_076915.2:p.Phe332Ser
XM_006714474.2:c.995T>C XP_006714537.1:p.Phe332Ser
XM_011514043.1:c.995T>C XP_011512345.1:p.Phe332Ser
XM_011514044.1:c.914T>C XP_011512346.1:p.Phe305Ser
XM_011514045.1:c.1135T>C XP_011512347.1:p.Phe379Leu
XR_241702.1:n.1017T>C
XR_241703.1:n.1010T>C
XR_925614.1:n.1017T>C
XR_925615.1:n.1017T>C
NM_001364440.1:c.914T>C NP_001351369.1:p.Phe305Ser
NM_001364441.1:c.914T>C NP_001351370.1:p.Phe305Ser
NM_001364442.1:c.914T>C NP_001351371.1:p.Phe305Ser
NM_024010.3:c.914T>C NP_076915.3:p.Phe305Ser
NR_134480.1:n.1037T>C
NR_134481.1:n.1051T>C
NR_134482.1:n.897T>C
NR_157168.1:n.967T>C
NR_157169.1:n.827T>C
NR_157170.1:n.993T>C
NR_157171.1:n.827T>C
NR_157172.1:n.853T>C
NR_157173.1:n.981T>C
NR_157174.1:n.853T>C
NR_157175.1:n.1007T>C
NR_157176.1:n.1147T>C
NR_157177.1:n.1002T>C
NR_157178.1:n.1007T>C
XM_024446063.1:c.959T>C XP_024301831.1:p.Phe320Ser
XM_024446064.1:c.914T>C XP_024301832.1:p.Phe305Ser
XR_001742071.1:n.1017T>C
XR_001742072.1:n.1017T>C
XR_001742074.1:n.1017T>C
XR_001742075.1:n.1017T>C
XR_001742076.1:n.1157T>C
XR_001742077.1:n.1157T>C
NM_001364440.2:c.914T>C NP_001351369.1:p.Phe305Ser
NM_001364441.2:c.914T>C NP_001351370.1:p.Phe305Ser
NM_001364442.2:c.914T>C NP_001351371.1:p.Phe305Ser
NM_002454.3:c.914T>C MANE Select NP_002445.2:p.Phe305Ser
NM_024010.4:c.914T>C NP_076915.3:p.Phe305Ser
NR_134480.2:n.993T>C
NR_134481.2:n.1007T>C
NR_134482.2:n.853T>C
NR_157168.2:n.967T>C
NR_157169.2:n.827T>C
NR_157170.2:n.993T>C
NR_157171.2:n.827T>C
NR_157172.2:n.853T>C
NR_157173.2:n.981T>C
NR_157174.2:n.853T>C
NR_157175.2:n.1007T>C
NR_157176.2:n.1147T>C
NR_157177.2:n.1002T>C
NR_157178.2:n.1007T>C