Canonical Allele Identifier: CA359156892

Gene: MTRR

Linked Data

• MyVariant Identifiers: chr5:g.7878169C>A (hg19) ; chr5:g.7878056C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7878056C>A , CM000667.2:g.7878056C>A	GRCh38
NC_000005.9:g.7878169C>A , CM000667.1:g.7878169C>A	GRCh37
NC_000005.8:g.7931169C>A	NCBI36
NG_008856.1:g.13953C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440940.7:c.514C>A MANE Select	ENSP00000402510.2:p.Pro172Thr
ENST00000264668.6:c.595C>A	ENSP00000264668.2:p.Pro199Thr
ENST00000440940.6:c.514C>A	ENSP00000402510.2:p.Pro172Thr
ENST00000508890.1:n.327C>A
ENST00000510279.5:c.*183C>A	ENSP00000427200.1:n.*183C>A
ENST00000510525.5:c.539C>A
ENST00000511461.5:c.427C>A
ENST00000513439.5:c.*221C>A	ENSP00000426710.1:n.*221C>A
ENST00000514220.5:c.299C>A
ENST00000514369.5:c.*178C>A	ENSP00000426132.1:n.*178C>A
NM_002454.2:c.514C>A	NP_002445.2:p.Pro172Thr
NM_024010.2:c.595C>A	NP_076915.2:p.Pro199Thr
XM_006714474.2:c.595C>A	XP_006714537.1:p.Pro199Thr
XM_011514043.1:c.595C>A	XP_011512345.1:p.Pro199Thr
XM_011514044.1:c.514C>A	XP_011512346.1:p.Pro172Thr
XM_011514045.1:c.595C>A	XP_011512347.1:p.Pro199Thr
XR_241702.1:n.617C>A
XR_241703.1:n.610C>A
XR_925614.1:n.617C>A
XR_925615.1:n.617C>A
NM_001364440.1:c.514C>A	NP_001351369.1:p.Pro172Thr
NM_001364441.1:c.514C>A	NP_001351370.1:p.Pro172Thr
NM_001364442.1:c.514C>A	NP_001351371.1:p.Pro172Thr
NM_024010.3:c.514C>A	NP_076915.3:p.Pro172Thr
NR_134480.1:n.637C>A
NR_134481.1:n.651C>A
NR_134482.1:n.497C>A
NR_157168.1:n.567C>A
NR_157169.1:n.427C>A
NR_157170.1:n.453C>A
NR_157171.1:n.427C>A
NR_157172.1:n.453C>A
NR_157173.1:n.581C>A
NR_157174.1:n.453C>A
NR_157175.1:n.607C>A
NR_157176.1:n.607C>A
NR_157177.1:n.602C>A
NR_157178.1:n.607C>A
XM_024446063.1:c.559C>A	XP_024301831.1:p.Pro187Thr
XM_024446064.1:c.514C>A	XP_024301832.1:p.Pro172Thr
XR_001742071.1:n.617C>A
XR_001742072.1:n.617C>A
XR_001742074.1:n.617C>A
XR_001742075.1:n.617C>A
XR_001742076.1:n.617C>A
XR_001742077.1:n.617C>A
NM_001364440.2:c.514C>A	NP_001351369.1:p.Pro172Thr
NM_001364441.2:c.514C>A	NP_001351370.1:p.Pro172Thr
NM_001364442.2:c.514C>A	NP_001351371.1:p.Pro172Thr
NM_002454.3:c.514C>A MANE Select	NP_002445.2:p.Pro172Thr
NM_024010.4:c.514C>A	NP_076915.3:p.Pro172Thr
NR_134480.2:n.593C>A
NR_134481.2:n.607C>A
NR_134482.2:n.453C>A
NR_157168.2:n.567C>A
NR_157169.2:n.427C>A
NR_157170.2:n.453C>A
NR_157171.2:n.427C>A
NR_157172.2:n.453C>A
NR_157173.2:n.581C>A
NR_157174.2:n.453C>A
NR_157175.2:n.607C>A
NR_157176.2:n.607C>A
NR_157177.2:n.602C>A
NR_157178.2:n.607C>A