Canonical Allele Identifier: CA814254694

Gene: MTRR

Linked Data

• dbSNP Id: rs1412918810
• gnomAD v3: 5-7885397-ATAGGACCTTACT-A
• gnomAD v4: 5-7885397-ATAGGACCTTACT-A
• MyVariant Identifiers: chr5:g.7885511_7885522del (hg19) ; chr5:g.7885398_7885409del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7885399_7885410del , CM000667.2:g.7885399_7885410del	GRCh38
NC_000005.9:g.7885512_7885523del , CM000667.1:g.7885512_7885523del	GRCh37
NC_000005.8:g.7938512_7938523del	NCBI36
NG_008856.1:g.21296_21307del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440940.7:c.904-302_904-291del MANE Select	ENSP00000402510.2:n.904-302_904-291del
ENST00000264668.6:c.985-302_985-291del	ENSP00000264668.2:n.985-302_985-291del
ENST00000440940.6:c.904-302_904-291del	ENSP00000402510.2:n.904-302_904-291del
ENST00000508101.5:n.143+141_143+152del
ENST00000510525.5:c.929-302_929-291del
ENST00000511461.5:c.817-302_817-291del
ENST00000513439.5:c.*611-302_*611-291del	ENSP00000426710.1:n.*611-302_*611-291del
NM_002454.2:c.904-302_904-291del	NP_002445.2:n.904-302_904-291del
NM_024010.2:c.985-302_985-291del	NP_076915.2:n.985-302_985-291del
XM_006714474.2:c.985-302_985-291del	XP_006714537.1:n.985-302_985-291del
XM_011514043.1:c.985-302_985-291del	XP_011512345.1:n.985-302_985-291del
XM_011514044.1:c.904-302_904-291del	XP_011512346.1:n.904-302_904-291del
XM_011514045.1:c.1125-302_1125-291del	XP_011512347.1:n.1125-302_1125-291del
XR_241702.1:n.1007-302_1007-291del
XR_241703.1:n.1000-302_1000-291del
XR_925614.1:n.1007-302_1007-291del
XR_925615.1:n.1007-302_1007-291del
NM_001364440.1:c.904-302_904-291del	NP_001351369.1:n.904-302_904-291del
NM_001364441.1:c.904-302_904-291del	NP_001351370.1:n.904-302_904-291del
NM_001364442.1:c.904-302_904-291del	NP_001351371.1:n.904-302_904-291del
NM_024010.3:c.904-302_904-291del	NP_076915.3:n.904-302_904-291del
NR_134480.1:n.1027-302_1027-291del
NR_134481.1:n.1041-302_1041-291del
NR_134482.1:n.887-302_887-291del
NR_157168.1:n.957-302_957-291del
NR_157169.1:n.817-302_817-291del
NR_157170.1:n.983-302_983-291del
NR_157171.1:n.817-302_817-291del
NR_157172.1:n.843-302_843-291del
NR_157173.1:n.971-302_971-291del
NR_157174.1:n.843-302_843-291del
NR_157175.1:n.997-302_997-291del
NR_157176.1:n.1137-302_1137-291del
NR_157177.1:n.992-302_992-291del
NR_157178.1:n.997-302_997-291del
XM_024446063.1:c.949-302_949-291del	XP_024301831.1:n.949-302_949-291del
XM_024446064.1:c.904-302_904-291del	XP_024301832.1:n.904-302_904-291del
XR_001742071.1:n.1007-302_1007-291del
XR_001742072.1:n.1007-302_1007-291del
XR_001742074.1:n.1007-302_1007-291del
XR_001742075.1:n.1007-302_1007-291del
XR_001742076.1:n.1147-302_1147-291del
XR_001742077.1:n.1147-302_1147-291del
NM_001364440.2:c.904-302_904-291del	NP_001351369.1:n.904-302_904-291del
NM_001364441.2:c.904-302_904-291del	NP_001351370.1:n.904-302_904-291del
NM_001364442.2:c.904-302_904-291del	NP_001351371.1:n.904-302_904-291del
NM_002454.3:c.904-302_904-291del MANE Select	NP_002445.2:n.904-302_904-291del
NM_024010.4:c.904-302_904-291del	NP_076915.3:n.904-302_904-291del
NR_134480.2:n.983-302_983-291del
NR_134481.2:n.997-302_997-291del
NR_134482.2:n.843-302_843-291del
NR_157168.2:n.957-302_957-291del
NR_157169.2:n.817-302_817-291del
NR_157170.2:n.983-302_983-291del
NR_157171.2:n.817-302_817-291del
NR_157172.2:n.843-302_843-291del
NR_157173.2:n.971-302_971-291del
NR_157174.2:n.843-302_843-291del
NR_157175.2:n.997-302_997-291del
NR_157176.2:n.1137-302_1137-291del
NR_157177.2:n.992-302_992-291del
NR_157178.2:n.997-302_997-291del