Canonical Allele Identifier: CA15681827
Gene: MRE11A HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1014666

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94445959T>C , CM000673.2:g.94445959T>C GRCh38
NC_000011.9:g.94179125T>C , CM000673.1:g.94179125T>C GRCh37
NC_000011.8:g.93818773T>C NCBI36
NG_007261.1:g.52916A>G , LRG_85:g.52916A>G

Transcript Alleles

HGVS Amino-acid change
NM_005590.3:c.1783+1260A>G VV NP_005581.2:p.=
NM_005591.3:c.1784-66A>G , LRG_85t1:c.1784-66A>G NP_005582.1:p.=
XM_005274008.2:c.1316-66A>G XP_005274065.1:p.=
XM_006718842.2:c.1784-69A>G XP_006718905.1:p.=
XM_011542837.1:c.1784-66A>G XP_011541139.1:p.=
XR_947828.1:n.2080-66A>G
NM_001330347.1:c.1784-69A>G VV NP_001317276.1:p.=
XM_005274008.3:c.1316-66A>G
XM_006718842.3:c.1784-69A>G
XM_011542837.2:c.1784-66A>G
XM_017017772.1:c.1784-66A>G XP_016873261.1:p.=
XR_947828.2:n.2080-66A>G
ENST00000323929.7:c.1784-66A>G ENSP00000325863.3:p.=
ENST00000323977.7:c.1783+1260A>G ENSP00000326094.3:p.=
ENST00000393241.8:c.1784-69A>G ENSP00000376933.4:p.=
ENST00000407439.7:c.1793-66A>G ENSP00000385614.3:p.=
ENST00000535120.1:n.83-69A>G