Canonical Allele Identifier: CA2573147776

Gene: MRE11

Linked Data

• ClinVar Variation Id: 1681591
• ClinVar RCV Id: RCV002239124 ; RCV002463148
• dbSNP Id: rs2134999194

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94464112_94464113delinsTG , CM000673.2:g.94464112_94464113delinsTG	GRCh38
NC_000011.9:g.94197278_94197279delinsTG , CM000673.1:g.94197278_94197279delinsTG	GRCh37
NC_000011.8:g.93836926_93836927delinsTG	NCBI36
NG_007261.1:g.34762_34763delinsCA , LRG_85:g.34762_34763delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000323929.8:c.1225_1225+1delinsCA
ENST00000323929.7:c.1225_1225+1delinsCA
ENST00000323977.7:c.1225_1225+1delinsCA
ENST00000393241.8:c.1225_1225+1delinsCA
ENST00000407439.7:c.1234_1234+1delinsCA
NM_005590.3:c.1225_1225+1delinsCA
NM_005591.3:c.1225_1225+1delinsCA , LRG_85t1:c.1225_1225+1delinsCA
XM_005274008.2:c.757_757+1delinsCA
XM_006718842.2:c.1225_1225+1delinsCA
XM_011542837.1:c.1225_1225+1delinsCA
XR_947828.1:n.1521_1521+1delinsCA
NM_001330347.1:c.1225_1225+1delinsCA
XM_005274008.3:c.757_757+1delinsCA
XM_006718842.3:c.1225_1225+1delinsCA
XM_011542837.2:c.1225_1225+1delinsCA
XM_017017772.1:c.1225_1225+1delinsCA
XR_947828.2:n.1521_1521+1delinsCA
NM_001330347.2:c.1225_1225+1delinsCA
NM_005590.4:c.1225_1225+1delinsCA
NM_005591.4:c.1225_1225+1delinsCA