Canonical Allele Identifier: CA1992448234
Gene: MRE11 HGNC NCBI

Linked Data

dbSNP Id: rs1945591822

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94435818dup , CM000673.2:g.94435818dup GRCh38
NC_000011.9:g.94168984dup , CM000673.1:g.94168984dup GRCh37
NC_000011.8:g.93808632dup NCBI36
NG_007261.1:g.63060dup , LRG_85:g.63060dup

Transcript Alleles

HGVS Amino-acid change
ENST00000323929.8:c.1994+17dup MANE Select ENSP00000325863.4:n.1994+17dup
ENST00000323929.7:c.1994+17dup ENSP00000325863.3:n.1994+17dup
ENST00000323977.7:c.1910+17dup ENSP00000326094.3:n.1910+17dup
ENST00000393241.8:c.1991+17dup ENSP00000376933.4:n.1991+17dup
ENST00000407439.7:c.2003+17dup ENSP00000385614.3:n.2003+17dup
NM_005590.3:c.1910+17dup NP_005581.2:n.1910+17dup
NM_005591.3:c.1994+17dup , LRG_85t1:c.1994+17dup NP_005582.1:n.1994+17dup
XM_005274008.2:c.1526+17dup XP_005274065.1:n.1526+17dup
XM_006718842.2:c.1991+17dup XP_006718905.1:n.1991+17dup
XM_011542837.1:c.1994+17dup XP_011541139.1:n.1994+17dup
XR_947828.1:n.2290+17dup
NM_001330347.1:c.1991+17dup NP_001317276.1:n.1991+17dup
XM_005274008.3:c.1526+17dup XP_005274065.1:n.1526+17dup
XM_006718842.3:c.1991+17dup XP_006718905.1:n.1991+17dup
XM_011542837.2:c.1994+17dup XP_011541139.1:n.1994+17dup
XM_017017772.1:c.1994+17dup XP_016873261.1:n.1994+17dup
XR_947828.2:n.2290+17dup
NM_001330347.2:c.1991+17dup NP_001317276.1:n.1991+17dup
NM_005590.4:c.1910+17dup NP_005581.2:n.1910+17dup
NM_005591.4:c.1994+17dup MANE Select NP_005582.1:n.1994+17dup