Canonical Allele Identifier: CA359156997

Gene: MTRR

Linked Data

• MyVariant Identifiers: chr5:g.7878220T>A (hg19) ; chr5:g.7878107T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7878107T>A , CM000667.2:g.7878107T>A	GRCh38
NC_000005.9:g.7878220T>A , CM000667.1:g.7878220T>A	GRCh37
NC_000005.8:g.7931220T>A	NCBI36
NG_008856.1:g.14004T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440940.7:c.565T>A MANE Select	ENSP00000402510.2:p.Ser189Thr
ENST00000264668.6:c.646T>A	ENSP00000264668.2:p.Ser216Thr
ENST00000440940.6:c.565T>A	ENSP00000402510.2:p.Ser189Thr
ENST00000510279.5:c.*234T>A	ENSP00000427200.1:n.*234T>A
ENST00000510525.5:c.590T>A
ENST00000511461.5:c.478T>A
ENST00000513439.5:c.*272T>A	ENSP00000426710.1:n.*272T>A
ENST00000514220.5:c.350T>A
ENST00000514369.5:c.*229T>A	ENSP00000426132.1:n.*229T>A
NM_002454.2:c.565T>A	NP_002445.2:p.Ser189Thr
NM_024010.2:c.646T>A	NP_076915.2:p.Ser216Thr
XM_006714474.2:c.646T>A	XP_006714537.1:p.Ser216Thr
XM_011514043.1:c.646T>A	XP_011512345.1:p.Ser216Thr
XM_011514044.1:c.565T>A	XP_011512346.1:p.Ser189Thr
XM_011514045.1:c.646T>A	XP_011512347.1:p.Ser216Thr
XR_241702.1:n.668T>A
XR_241703.1:n.661T>A
XR_925614.1:n.668T>A
XR_925615.1:n.668T>A
NM_001364440.1:c.565T>A	NP_001351369.1:p.Ser189Thr
NM_001364441.1:c.565T>A	NP_001351370.1:p.Ser189Thr
NM_001364442.1:c.565T>A	NP_001351371.1:p.Ser189Thr
NM_024010.3:c.565T>A	NP_076915.3:p.Ser189Thr
NR_134480.1:n.688T>A
NR_134481.1:n.702T>A
NR_134482.1:n.548T>A
NR_157168.1:n.618T>A
NR_157169.1:n.478T>A
NR_157170.1:n.504T>A
NR_157171.1:n.478T>A
NR_157172.1:n.504T>A
NR_157173.1:n.632T>A
NR_157174.1:n.504T>A
NR_157175.1:n.658T>A
NR_157176.1:n.658T>A
NR_157177.1:n.653T>A
NR_157178.1:n.658T>A
XM_024446063.1:c.610T>A	XP_024301831.1:p.Ser204Thr
XM_024446064.1:c.565T>A	XP_024301832.1:p.Ser189Thr
XR_001742071.1:n.668T>A
XR_001742072.1:n.668T>A
XR_001742074.1:n.668T>A
XR_001742075.1:n.668T>A
XR_001742076.1:n.668T>A
XR_001742077.1:n.668T>A
NM_001364440.2:c.565T>A	NP_001351369.1:p.Ser189Thr
NM_001364441.2:c.565T>A	NP_001351370.1:p.Ser189Thr
NM_001364442.2:c.565T>A	NP_001351371.1:p.Ser189Thr
NM_002454.3:c.565T>A MANE Select	NP_002445.2:p.Ser189Thr
NM_024010.4:c.565T>A	NP_076915.3:p.Ser189Thr
NR_134480.2:n.644T>A
NR_134481.2:n.658T>A
NR_134482.2:n.504T>A
NR_157168.2:n.618T>A
NR_157169.2:n.478T>A
NR_157170.2:n.504T>A
NR_157171.2:n.478T>A
NR_157172.2:n.504T>A
NR_157173.2:n.632T>A
NR_157174.2:n.504T>A
NR_157175.2:n.658T>A
NR_157176.2:n.658T>A
NR_157177.2:n.653T>A
NR_157178.2:n.658T>A