Canonical Allele Identifier: CA359158004

Gene: MTRR

Linked Data

• MyVariant Identifiers: chr5:g.7885937T>A (hg19) ; chr5:g.7885824T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7885824T>A , CM000667.2:g.7885824T>A	GRCh38
NC_000005.9:g.7885937T>A , CM000667.1:g.7885937T>A	GRCh37
NC_000005.8:g.7938937T>A	NCBI36
NG_008856.1:g.21721T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440940.7:c.1027T>A MANE Select	ENSP00000402510.2:p.Leu343Met
ENST00000264668.6:c.1108T>A	ENSP00000264668.2:p.Leu370Met
ENST00000440940.6:c.1027T>A	ENSP00000402510.2:p.Leu343Met
ENST00000508101.5:n.267T>A
ENST00000509961.5:n.40T>A
ENST00000510525.5:c.1052T>A
ENST00000511461.5:c.940T>A
ENST00000513439.5:c.*734T>A	ENSP00000426710.1:n.*734T>A
NM_002454.2:c.1027T>A	NP_002445.2:p.Leu343Met
NM_024010.2:c.1108T>A	NP_076915.2:p.Leu370Met
XM_006714474.2:c.1108T>A	XP_006714537.1:p.Leu370Met
XM_011514043.1:c.1108T>A	XP_011512345.1:p.Leu370Met
XM_011514044.1:c.1027T>A	XP_011512346.1:p.Leu343Met
XM_011514045.1:c.*81T>A	XP_011512347.1:n.*81T>A
XR_241702.1:n.1130T>A
XR_241703.1:n.1123T>A
XR_925614.1:n.1130T>A
XR_925615.1:n.1130T>A
NM_001364440.1:c.1027T>A	NP_001351369.1:p.Leu343Met
NM_001364441.1:c.1027T>A	NP_001351370.1:p.Leu343Met
NM_001364442.1:c.1027T>A	NP_001351371.1:p.Leu343Met
NM_024010.3:c.1027T>A	NP_076915.3:p.Leu343Met
NR_134480.1:n.1150T>A
NR_134481.1:n.1164T>A
NR_134482.1:n.1010T>A
NR_157168.1:n.1080T>A
NR_157169.1:n.940T>A
NR_157170.1:n.1106T>A
NR_157171.1:n.940T>A
NR_157172.1:n.966T>A
NR_157173.1:n.1094T>A
NR_157174.1:n.966T>A
NR_157175.1:n.1120T>A
NR_157176.1:n.1260T>A
NR_157177.1:n.1115T>A
NR_157178.1:n.1120T>A
XM_024446063.1:c.1072T>A	XP_024301831.1:p.Leu358Met
XM_024446064.1:c.1027T>A	XP_024301832.1:p.Leu343Met
XR_001742071.1:n.1130T>A
XR_001742072.1:n.1130T>A
XR_001742074.1:n.1130T>A
XR_001742075.1:n.1130T>A
XR_001742076.1:n.1270T>A
XR_001742077.1:n.1270T>A
NM_001364440.2:c.1027T>A	NP_001351369.1:p.Leu343Met
NM_001364441.2:c.1027T>A	NP_001351370.1:p.Leu343Met
NM_001364442.2:c.1027T>A	NP_001351371.1:p.Leu343Met
NM_002454.3:c.1027T>A MANE Select	NP_002445.2:p.Leu343Met
NM_024010.4:c.1027T>A	NP_076915.3:p.Leu343Met
NR_134480.2:n.1106T>A
NR_134481.2:n.1120T>A
NR_134482.2:n.966T>A
NR_157168.2:n.1080T>A
NR_157169.2:n.940T>A
NR_157170.2:n.1106T>A
NR_157171.2:n.940T>A
NR_157172.2:n.966T>A
NR_157173.2:n.1094T>A
NR_157174.2:n.966T>A
NR_157175.2:n.1120T>A
NR_157176.2:n.1260T>A
NR_157177.2:n.1115T>A
NR_157178.2:n.1120T>A