Canonical Allele Identifier: CA119921
Gene: MRE11A HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 8783
dbSNP Id: rs137852760

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94479726T>C , CM000673.2:g.94479726T>C GRCh38
NC_000011.8:g.93852540T>C NCBI36
NC_000011.9:g.94212892T>C , CM000673.1:g.94212892T>C GRCh37
NG_007261.1:g.19149A>G , LRG_85:g.19149A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000323929.7:c.350A>G ENSP00000325863.3:p.Asn117Ser
ENST00000323977.7:c.350A>G ENSP00000326094.3:p.Asn117Ser
ENST00000393241.8:c.350A>G ENSP00000376933.4:p.Asn117Ser
ENST00000407439.7:c.359A>G ENSP00000385614.3:p.Asn120Ser
ENST00000536754.5:c.350A>G ENSP00000439511.1:p.Asn117Ser
ENST00000540013.5:c.350A>G ENSP00000440986.1:p.Asn117Ser
ENST00000541157.5:n.479-850A>G
NM_005590.3:c.350A>G VV NP_005581.2:p.Asn117Ser
NM_005591.3:c.350A>G , LRG_85t1:c.350A>G NP_005582.1:p.Asn117Ser
XM_005274008.2:c.-119A>G XP_005274065.1:p.=
XM_006718842.2:c.350A>G XP_006718905.1:p.Asn117Ser
XM_011542837.1:c.350A>G XP_011541139.1:p.Asn117Ser
XR_947828.1:n.646A>G
NM_001330347.1:c.350A>G VV NP_001317276.1:p.Asn117Ser
XM_005274008.3:c.-119A>G
XM_006718842.3:c.350A>G
XM_011542837.2:c.350A>G
XM_017017772.1:c.350A>G XP_016873261.1:p.Asn117Ser
XR_947828.2:n.646A>G