Canonical Allele Identifier: CA1525806838

Gene: MTRR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7900599G= , CM000667.2:g.7900599G=	GRCh38
NC_000005.9:g.7900712G= , CM000667.1:g.7900712G=	GRCh37
NC_000005.8:g.7953712G=	NCBI36
NG_008856.1:g.36496G=

Transcript Alleles

HGVS	Amino-acid Change
NM_002454.3:c.*541G= MANE Select	NP_002445.2:n.*541G=
ENST00000440940.7:c.*541G= MANE Select	ENSP00000402510.2:n.*541G=
NM_001364440.1:c.*541G=	NP_001351369.1:n.*541G=
NM_001364440.2:c.*541G=	NP_001351369.1:n.*541G=
NM_001364441.1:c.*541G=	NP_001351370.1:n.*541G=
NM_001364441.2:c.*541G=	NP_001351370.1:n.*541G=
NM_001364442.1:c.*541G=	NP_001351371.1:n.*541G=
NM_001364442.2:c.*541G=	NP_001351371.1:n.*541G=
NM_002454.2:c.*541G=	NP_002445.2:n.*541G=
NM_024010.2:c.*541G=	NP_076915.2:n.*541G=
NM_024010.3:c.*541G=	NP_076915.3:n.*541G=
NM_024010.4:c.*541G=	NP_076915.3:n.*541G=
NR_134480.1:n.2761G=
NR_134480.2:n.2717G=
NR_134481.1:n.2686G=
NR_134481.2:n.2642G=
NR_134482.1:n.2621G=
NR_134482.2:n.2577G=
NR_157168.1:n.2691G=
NR_157168.2:n.2691G=
NR_157169.1:n.2551G=
NR_157169.2:n.2551G=
NR_157170.1:n.2717G=
NR_157170.2:n.2717G=
NR_157171.1:n.2574G=
NR_157171.2:n.2574G=
NR_157172.1:n.2488G=
NR_157172.2:n.2488G=
NR_157173.1:n.2728G=
NR_157173.2:n.2728G=
NR_157174.1:n.2729G=
NR_157174.2:n.2729G=
NR_157175.1:n.2883G=
NR_157175.2:n.2883G=
NR_157176.1:n.3046G=
NR_157176.2:n.3046G=
NR_157177.1:n.2726G=
NR_157177.2:n.2726G=
NR_157178.1:n.2754G=
NR_157178.2:n.2754G=
ENST00000264668.6:c.*541G=	ENSP00000264668.2:n.*541G=
ENST00000440940.6:c.*541G=	ENSP00000402510.2:n.*541G=
ENST00000506115.1:n.543+142G=
ENST00000510525.5:c.2574G=
ENST00000511461.5:c.2551G=
XM_011514044.1:c.*541G=	XP_011512346.1:n.*541G=
XM_024446063.1:c.*541G=	XP_024301831.1:n.*541G=
XM_024446064.1:c.*541G=	XP_024301832.1:n.*541G=
XR_001742071.1:n.2916G=
XR_001742072.1:n.2893G=
XR_001742074.1:n.2652G=
XR_001742075.1:n.2804G=
XR_001742076.1:n.2881G=
XR_001742077.1:n.2904G=
XR_241703.1:n.2645G=
XR_925614.1:n.2764G=