Canonical Allele Identifier: CA359157086

Gene: MTRR

Linked Data

• ClinVar Variation Id: 618732
• ClinVar RCV Id: RCV000757494
• dbSNP Id: rs1561185945
• MyVariant Identifiers: chr5:g.7878262G>T (hg19) ; chr5:g.7878149G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7878149G>T , CM000667.2:g.7878149G>T	GRCh38
NC_000005.9:g.7878262G>T , CM000667.1:g.7878262G>T	GRCh37
NC_000005.8:g.7931262G>T	NCBI36
NG_008856.1:g.14046G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440940.7:c.607G>T MANE Select	ENSP00000402510.2:p.Asp203Tyr
ENST00000264668.6:c.688G>T	ENSP00000264668.2:p.Asp230Tyr
ENST00000440940.6:c.607G>T	ENSP00000402510.2:p.Asp203Tyr
ENST00000510279.5:c.*276G>T	ENSP00000427200.1:n.*276G>T
ENST00000510525.5:c.632G>T
ENST00000511461.5:c.520G>T
ENST00000513439.5:c.*314G>T	ENSP00000426710.1:n.*314G>T
ENST00000514220.5:c.392G>T
ENST00000514369.5:c.*271G>T	ENSP00000426132.1:n.*271G>T
NM_002454.2:c.607G>T	NP_002445.2:p.Asp203Tyr
NM_024010.2:c.688G>T	NP_076915.2:p.Asp230Tyr
XM_006714474.2:c.688G>T	XP_006714537.1:p.Asp230Tyr
XM_011514043.1:c.688G>T	XP_011512345.1:p.Asp230Tyr
XM_011514044.1:c.607G>T	XP_011512346.1:p.Asp203Tyr
XM_011514045.1:c.688G>T	XP_011512347.1:p.Asp230Tyr
XR_241702.1:n.710G>T
XR_241703.1:n.703G>T
XR_925614.1:n.710G>T
XR_925615.1:n.710G>T
NM_001364440.1:c.607G>T	NP_001351369.1:p.Asp203Tyr
NM_001364441.1:c.607G>T	NP_001351370.1:p.Asp203Tyr
NM_001364442.1:c.607G>T	NP_001351371.1:p.Asp203Tyr
NM_024010.3:c.607G>T	NP_076915.3:p.Asp203Tyr
NR_134480.1:n.730G>T
NR_134481.1:n.744G>T
NR_134482.1:n.590G>T
NR_157168.1:n.660G>T
NR_157169.1:n.520G>T
NR_157170.1:n.546G>T
NR_157171.1:n.520G>T
NR_157172.1:n.546G>T
NR_157173.1:n.674G>T
NR_157174.1:n.546G>T
NR_157175.1:n.700G>T
NR_157176.1:n.700G>T
NR_157177.1:n.695G>T
NR_157178.1:n.700G>T
XM_024446063.1:c.652G>T	XP_024301831.1:p.Asp218Tyr
XM_024446064.1:c.607G>T	XP_024301832.1:p.Asp203Tyr
XR_001742071.1:n.710G>T
XR_001742072.1:n.710G>T
XR_001742074.1:n.710G>T
XR_001742075.1:n.710G>T
XR_001742076.1:n.710G>T
XR_001742077.1:n.710G>T
NM_001364440.2:c.607G>T	NP_001351369.1:p.Asp203Tyr
NM_001364441.2:c.607G>T	NP_001351370.1:p.Asp203Tyr
NM_001364442.2:c.607G>T	NP_001351371.1:p.Asp203Tyr
NM_002454.3:c.607G>T MANE Select	NP_002445.2:p.Asp203Tyr
NM_024010.4:c.607G>T	NP_076915.3:p.Asp203Tyr
NR_134480.2:n.686G>T
NR_134481.2:n.700G>T
NR_134482.2:n.546G>T
NR_157168.2:n.660G>T
NR_157169.2:n.520G>T
NR_157170.2:n.546G>T
NR_157171.2:n.520G>T
NR_157172.2:n.546G>T
NR_157173.2:n.674G>T
NR_157174.2:n.546G>T
NR_157175.2:n.700G>T
NR_157176.2:n.700G>T
NR_157177.2:n.695G>T
NR_157178.2:n.700G>T