Canonical Allele Identifier: CA814254725

Gene: MTRR

Linked Data

• dbSNP Id: rs1240474816
• MyVariant Identifiers: chr5:g.7885586_7885589del (hg19) ; chr5:g.7885473_7885476del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7885475_7885478del , CM000667.2:g.7885475_7885478del	GRCh38
NC_000005.9:g.7885588_7885591del , CM000667.1:g.7885588_7885591del	GRCh37
NC_000005.8:g.7938588_7938591del	NCBI36
NG_008856.1:g.21372_21375del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440940.7:c.904-226_904-223del MANE Select	ENSP00000402510.2:n.904-226_904-223del
ENST00000264668.6:c.985-226_985-223del	ENSP00000264668.2:n.985-226_985-223del
ENST00000440940.6:c.904-226_904-223del	ENSP00000402510.2:n.904-226_904-223del
ENST00000508101.5:n.143+217_143+220del
ENST00000510525.5:c.929-226_929-223del
ENST00000511461.5:c.817-226_817-223del
ENST00000513439.5:c.*611-226_*611-223del	ENSP00000426710.1:n.*611-226_*611-223del
NM_002454.2:c.904-226_904-223del	NP_002445.2:n.904-226_904-223del
NM_024010.2:c.985-226_985-223del	NP_076915.2:n.985-226_985-223del
XM_006714474.2:c.985-226_985-223del	XP_006714537.1:n.985-226_985-223del
XM_011514043.1:c.985-226_985-223del	XP_011512345.1:n.985-226_985-223del
XM_011514044.1:c.904-226_904-223del	XP_011512346.1:n.904-226_904-223del
XM_011514045.1:c.1125-226_1125-223del	XP_011512347.1:n.1125-226_1125-223del
XR_241702.1:n.1007-226_1007-223del
XR_241703.1:n.1000-226_1000-223del
XR_925614.1:n.1007-226_1007-223del
XR_925615.1:n.1007-226_1007-223del
NM_001364440.1:c.904-226_904-223del	NP_001351369.1:n.904-226_904-223del
NM_001364441.1:c.904-226_904-223del	NP_001351370.1:n.904-226_904-223del
NM_001364442.1:c.904-226_904-223del	NP_001351371.1:n.904-226_904-223del
NM_024010.3:c.904-226_904-223del	NP_076915.3:n.904-226_904-223del
NR_134480.1:n.1027-226_1027-223del
NR_134481.1:n.1041-226_1041-223del
NR_134482.1:n.887-226_887-223del
NR_157168.1:n.957-226_957-223del
NR_157169.1:n.817-226_817-223del
NR_157170.1:n.983-226_983-223del
NR_157171.1:n.817-226_817-223del
NR_157172.1:n.843-226_843-223del
NR_157173.1:n.971-226_971-223del
NR_157174.1:n.843-226_843-223del
NR_157175.1:n.997-226_997-223del
NR_157176.1:n.1137-226_1137-223del
NR_157177.1:n.992-226_992-223del
NR_157178.1:n.997-226_997-223del
XM_024446063.1:c.949-226_949-223del	XP_024301831.1:n.949-226_949-223del
XM_024446064.1:c.904-226_904-223del	XP_024301832.1:n.904-226_904-223del
XR_001742071.1:n.1007-226_1007-223del
XR_001742072.1:n.1007-226_1007-223del
XR_001742074.1:n.1007-226_1007-223del
XR_001742075.1:n.1007-226_1007-223del
XR_001742076.1:n.1147-226_1147-223del
XR_001742077.1:n.1147-226_1147-223del
NM_001364440.2:c.904-226_904-223del	NP_001351369.1:n.904-226_904-223del
NM_001364441.2:c.904-226_904-223del	NP_001351370.1:n.904-226_904-223del
NM_001364442.2:c.904-226_904-223del	NP_001351371.1:n.904-226_904-223del
NM_002454.3:c.904-226_904-223del MANE Select	NP_002445.2:n.904-226_904-223del
NM_024010.4:c.904-226_904-223del	NP_076915.3:n.904-226_904-223del
NR_134480.2:n.983-226_983-223del
NR_134481.2:n.997-226_997-223del
NR_134482.2:n.843-226_843-223del
NR_157168.2:n.957-226_957-223del
NR_157169.2:n.817-226_817-223del
NR_157170.2:n.983-226_983-223del
NR_157171.2:n.817-226_817-223del
NR_157172.2:n.843-226_843-223del
NR_157173.2:n.971-226_971-223del
NR_157174.2:n.843-226_843-223del
NR_157175.2:n.997-226_997-223del
NR_157176.2:n.1137-226_1137-223del
NR_157177.2:n.992-226_992-223del
NR_157178.2:n.997-226_997-223del