Canonical Allele Identifier: CA359157072

Gene: MTRR

Linked Data

• MyVariant Identifiers: chr5:g.7878256A>T (hg19) ; chr5:g.7878143A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7878143A>T , CM000667.2:g.7878143A>T	GRCh38
NC_000005.9:g.7878256A>T , CM000667.1:g.7878256A>T	GRCh37
NC_000005.8:g.7931256A>T	NCBI36
NG_008856.1:g.14040A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440940.7:c.601A>T MANE Select	ENSP00000402510.2:p.Arg201Ter
ENST00000264668.6:c.682A>T	ENSP00000264668.2:p.Arg228Ter
ENST00000440940.6:c.601A>T	ENSP00000402510.2:p.Arg201Ter
ENST00000510279.5:c.*270A>T	ENSP00000427200.1:n.*270A>T
ENST00000510525.5:c.626A>T
ENST00000511461.5:c.514A>T
ENST00000513439.5:c.*308A>T	ENSP00000426710.1:n.*308A>T
ENST00000514220.5:c.386A>T
ENST00000514369.5:c.*265A>T	ENSP00000426132.1:n.*265A>T
NM_002454.2:c.601A>T	NP_002445.2:p.Arg201Ter
NM_024010.2:c.682A>T	NP_076915.2:p.Arg228Ter
XM_006714474.2:c.682A>T	XP_006714537.1:p.Arg228Ter
XM_011514043.1:c.682A>T	XP_011512345.1:p.Arg228Ter
XM_011514044.1:c.601A>T	XP_011512346.1:p.Arg201Ter
XM_011514045.1:c.682A>T	XP_011512347.1:p.Arg228Ter
XR_241702.1:n.704A>T
XR_241703.1:n.697A>T
XR_925614.1:n.704A>T
XR_925615.1:n.704A>T
NM_001364440.1:c.601A>T	NP_001351369.1:p.Arg201Ter
NM_001364441.1:c.601A>T	NP_001351370.1:p.Arg201Ter
NM_001364442.1:c.601A>T	NP_001351371.1:p.Arg201Ter
NM_024010.3:c.601A>T	NP_076915.3:p.Arg201Ter
NR_134480.1:n.724A>T
NR_134481.1:n.738A>T
NR_134482.1:n.584A>T
NR_157168.1:n.654A>T
NR_157169.1:n.514A>T
NR_157170.1:n.540A>T
NR_157171.1:n.514A>T
NR_157172.1:n.540A>T
NR_157173.1:n.668A>T
NR_157174.1:n.540A>T
NR_157175.1:n.694A>T
NR_157176.1:n.694A>T
NR_157177.1:n.689A>T
NR_157178.1:n.694A>T
XM_024446063.1:c.646A>T	XP_024301831.1:p.Arg216Ter
XM_024446064.1:c.601A>T	XP_024301832.1:p.Arg201Ter
XR_001742071.1:n.704A>T
XR_001742072.1:n.704A>T
XR_001742074.1:n.704A>T
XR_001742075.1:n.704A>T
XR_001742076.1:n.704A>T
XR_001742077.1:n.704A>T
NM_001364440.2:c.601A>T	NP_001351369.1:p.Arg201Ter
NM_001364441.2:c.601A>T	NP_001351370.1:p.Arg201Ter
NM_001364442.2:c.601A>T	NP_001351371.1:p.Arg201Ter
NM_002454.3:c.601A>T MANE Select	NP_002445.2:p.Arg201Ter
NM_024010.4:c.601A>T	NP_076915.3:p.Arg201Ter
NR_134480.2:n.680A>T
NR_134481.2:n.694A>T
NR_134482.2:n.540A>T
NR_157168.2:n.654A>T
NR_157169.2:n.514A>T
NR_157170.2:n.540A>T
NR_157171.2:n.514A>T
NR_157172.2:n.540A>T
NR_157173.2:n.668A>T
NR_157174.2:n.540A>T
NR_157175.2:n.694A>T
NR_157176.2:n.694A>T
NR_157177.2:n.689A>T
NR_157178.2:n.694A>T