Canonical Allele Identifier: CA1525807816

Gene: MTRR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7901117T= , CM000667.2:g.7901117T=	GRCh38
NC_000005.9:g.7901230T= , CM000667.1:g.7901230T=	GRCh37
NC_000005.8:g.7954230T=	NCBI36
NG_008856.1:g.37014T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264668.6:c.*1059T=	ENSP00000264668.2:n.*1059T=
ENST00000440940.6:c.*1059T=	ENSP00000402510.2:n.*1059T=
ENST00000506115.1:n.618T=
ENST00000509379.1:n.51T=
ENST00000511461.5:c.3069T=
NM_002454.2:c.*1059T=	NP_002445.2:n.*1059T=
NM_024010.2:c.*1059T=	NP_076915.2:n.*1059T=
XM_011514044.1:c.*1059T=	XP_011512346.1:n.*1059T=
XR_241703.1:n.3163T=
XR_925614.1:n.3282T=
NM_001364440.1:c.*1059T=	NP_001351369.1:n.*1059T=
NM_001364441.1:c.*1059T=	NP_001351370.1:n.*1059T=
NM_001364442.1:c.*1059T=	NP_001351371.1:n.*1059T=
NM_024010.3:c.*1059T=	NP_076915.3:n.*1059T=
NR_134480.1:n.3279T=
NR_134481.1:n.3204T=
NR_134482.1:n.3139T=
NR_157168.1:n.3209T=
NR_157169.1:n.3069T=
NR_157170.1:n.3235T=
NR_157171.1:n.3092T=
NR_157172.1:n.3006T=
NR_157173.1:n.3246T=
NR_157174.1:n.3247T=
NR_157175.1:n.3401T=
NR_157176.1:n.3564T=
NR_157177.1:n.3244T=
NR_157178.1:n.3272T=
XM_024446063.1:c.*1059T=	XP_024301831.1:n.*1059T=
XM_024446064.1:c.*1059T=	XP_024301832.1:n.*1059T=
XR_001742071.1:n.3434T=
XR_001742072.1:n.3411T=
XR_001742074.1:n.3170T=
XR_001742075.1:n.3322T=
XR_001742076.1:n.3399T=
XR_001742077.1:n.3422T=