Canonical Allele Identifier: CA359157781

Gene: MTRR

Linked Data

• gnomAD v4: 5-7885722-C-G
• MyVariant Identifiers: chr5:g.7885835C>G (hg19) ; chr5:g.7885722C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7885722C>G , CM000667.2:g.7885722C>G	GRCh38
NC_000005.9:g.7885835C>G , CM000667.1:g.7885835C>G	GRCh37
NC_000005.8:g.7938835C>G	NCBI36
NG_008856.1:g.21619C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440940.7:c.925C>G MANE Select	ENSP00000402510.2:p.Pro309Ala
ENST00000264668.6:c.1006C>G	ENSP00000264668.2:p.Pro336Ala
ENST00000440940.6:c.925C>G	ENSP00000402510.2:p.Pro309Ala
ENST00000508101.5:n.165C>G
ENST00000510525.5:c.950C>G
ENST00000511461.5:c.838C>G
ENST00000513439.5:c.*632C>G	ENSP00000426710.1:n.*632C>G
NM_002454.2:c.925C>G	NP_002445.2:p.Pro309Ala
NM_024010.2:c.1006C>G	NP_076915.2:p.Pro336Ala
XM_006714474.2:c.1006C>G	XP_006714537.1:p.Pro336Ala
XM_011514043.1:c.1006C>G	XP_011512345.1:p.Pro336Ala
XM_011514044.1:c.925C>G	XP_011512346.1:p.Pro309Ala
XM_011514045.1:c.1146C>G	XP_011512347.1:p.Ser382Arg
XR_241702.1:n.1028C>G
XR_241703.1:n.1021C>G
XR_925614.1:n.1028C>G
XR_925615.1:n.1028C>G
NM_001364440.1:c.925C>G	NP_001351369.1:p.Pro309Ala
NM_001364441.1:c.925C>G	NP_001351370.1:p.Pro309Ala
NM_001364442.1:c.925C>G	NP_001351371.1:p.Pro309Ala
NM_024010.3:c.925C>G	NP_076915.3:p.Pro309Ala
NR_134480.1:n.1048C>G
NR_134481.1:n.1062C>G
NR_134482.1:n.908C>G
NR_157168.1:n.978C>G
NR_157169.1:n.838C>G
NR_157170.1:n.1004C>G
NR_157171.1:n.838C>G
NR_157172.1:n.864C>G
NR_157173.1:n.992C>G
NR_157174.1:n.864C>G
NR_157175.1:n.1018C>G
NR_157176.1:n.1158C>G
NR_157177.1:n.1013C>G
NR_157178.1:n.1018C>G
XM_024446063.1:c.970C>G	XP_024301831.1:p.Pro324Ala
XM_024446064.1:c.925C>G	XP_024301832.1:p.Pro309Ala
XR_001742071.1:n.1028C>G
XR_001742072.1:n.1028C>G
XR_001742074.1:n.1028C>G
XR_001742075.1:n.1028C>G
XR_001742076.1:n.1168C>G
XR_001742077.1:n.1168C>G
NM_001364440.2:c.925C>G	NP_001351369.1:p.Pro309Ala
NM_001364441.2:c.925C>G	NP_001351370.1:p.Pro309Ala
NM_001364442.2:c.925C>G	NP_001351371.1:p.Pro309Ala
NM_002454.3:c.925C>G MANE Select	NP_002445.2:p.Pro309Ala
NM_024010.4:c.925C>G	NP_076915.3:p.Pro309Ala
NR_134480.2:n.1004C>G
NR_134481.2:n.1018C>G
NR_134482.2:n.864C>G
NR_157168.2:n.978C>G
NR_157169.2:n.838C>G
NR_157170.2:n.1004C>G
NR_157171.2:n.838C>G
NR_157172.2:n.864C>G
NR_157173.2:n.992C>G
NR_157174.2:n.864C>G
NR_157175.2:n.1018C>G
NR_157176.2:n.1158C>G
NR_157177.2:n.1013C>G
NR_157178.2:n.1018C>G