Canonical Allele Identifier: CA359157802

Gene: MTRR

Linked Data

• gnomAD v4: 5-7885732-C-T
• MyVariant Identifiers: chr5:g.7885845C>T (hg19) ; chr5:g.7885732C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7885732C>T , CM000667.2:g.7885732C>T	GRCh38
NC_000005.9:g.7885845C>T , CM000667.1:g.7885845C>T	GRCh37
NC_000005.8:g.7938845C>T	NCBI36
NG_008856.1:g.21629C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440940.7:c.935C>T MANE Select	ENSP00000402510.2:p.Ala312Val
ENST00000264668.6:c.1016C>T	ENSP00000264668.2:p.Ala339Val
ENST00000440940.6:c.935C>T	ENSP00000402510.2:p.Ala312Val
ENST00000508101.5:n.175C>T
ENST00000510525.5:c.960C>T
ENST00000511461.5:c.848C>T
ENST00000513439.5:c.*642C>T	ENSP00000426710.1:n.*642C>T
NM_002454.2:c.935C>T	NP_002445.2:p.Ala312Val
NM_024010.2:c.1016C>T	NP_076915.2:p.Ala339Val
XM_006714474.2:c.1016C>T	XP_006714537.1:p.Ala339Val
XM_011514043.1:c.1016C>T	XP_011512345.1:p.Ala339Val
XM_011514044.1:c.935C>T	XP_011512346.1:p.Ala312Val
XM_011514045.1:c.1156C>T	XP_011512347.1:p.Pro386Ser
XR_241702.1:n.1038C>T
XR_241703.1:n.1031C>T
XR_925614.1:n.1038C>T
XR_925615.1:n.1038C>T
NM_001364440.1:c.935C>T	NP_001351369.1:p.Ala312Val
NM_001364441.1:c.935C>T	NP_001351370.1:p.Ala312Val
NM_001364442.1:c.935C>T	NP_001351371.1:p.Ala312Val
NM_024010.3:c.935C>T	NP_076915.3:p.Ala312Val
NR_134480.1:n.1058C>T
NR_134481.1:n.1072C>T
NR_134482.1:n.918C>T
NR_157168.1:n.988C>T
NR_157169.1:n.848C>T
NR_157170.1:n.1014C>T
NR_157171.1:n.848C>T
NR_157172.1:n.874C>T
NR_157173.1:n.1002C>T
NR_157174.1:n.874C>T
NR_157175.1:n.1028C>T
NR_157176.1:n.1168C>T
NR_157177.1:n.1023C>T
NR_157178.1:n.1028C>T
XM_024446063.1:c.980C>T	XP_024301831.1:p.Ala327Val
XM_024446064.1:c.935C>T	XP_024301832.1:p.Ala312Val
XR_001742071.1:n.1038C>T
XR_001742072.1:n.1038C>T
XR_001742074.1:n.1038C>T
XR_001742075.1:n.1038C>T
XR_001742076.1:n.1178C>T
XR_001742077.1:n.1178C>T
NM_001364440.2:c.935C>T	NP_001351369.1:p.Ala312Val
NM_001364441.2:c.935C>T	NP_001351370.1:p.Ala312Val
NM_001364442.2:c.935C>T	NP_001351371.1:p.Ala312Val
NM_002454.3:c.935C>T MANE Select	NP_002445.2:p.Ala312Val
NM_024010.4:c.935C>T	NP_076915.3:p.Ala312Val
NR_134480.2:n.1014C>T
NR_134481.2:n.1028C>T
NR_134482.2:n.874C>T
NR_157168.2:n.988C>T
NR_157169.2:n.848C>T
NR_157170.2:n.1014C>T
NR_157171.2:n.848C>T
NR_157172.2:n.874C>T
NR_157173.2:n.1002C>T
NR_157174.2:n.874C>T
NR_157175.2:n.1028C>T
NR_157176.2:n.1168C>T
NR_157177.2:n.1023C>T
NR_157178.2:n.1028C>T