Canonical Allele Identifier: CA6235391
Gene: MRE11 HGNC NCBI

Linked Data

ClinVar Variation Id: 847927
ClinVar RCV Id: RCV001051570
dbSNP Id: rs771615477

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94478845C>A , CM000673.2:g.94478845C>A GRCh38
NC_000011.9:g.94212011C>A , CM000673.1:g.94212011C>A GRCh37
NC_000011.8:g.93851659C>A NCBI36
NG_007261.1:g.20030G>T , LRG_85:g.20030G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000323929.8:c.434G>T MANE Select ENSP00000325863.4:p.Ser145Ile
ENST00000323929.7:c.434G>T ENSP00000325863.3:p.Ser145Ile
ENST00000323977.7:c.434G>T ENSP00000326094.3:p.Ser145Ile
ENST00000393241.8:c.434G>T ENSP00000376933.4:p.Ser145Ile
ENST00000407439.7:c.443G>T ENSP00000385614.3:p.Ser148Ile
ENST00000540013.5:c.434G>T ENSP00000440986.1:p.Ser145Ile
ENST00000541157.5:n.510G>T
NM_005590.3:c.434G>T NP_005581.2:p.Ser145Ile
NM_005591.3:c.434G>T , LRG_85t1:c.434G>T NP_005582.1:p.Ser145Ile
XM_005274008.2:c.-35G>T XP_005274065.1:n.-35G>T
XM_006718842.2:c.434G>T XP_006718905.1:p.Ser145Ile
XM_011542837.1:c.434G>T XP_011541139.1:p.Ser145Ile
XR_947828.1:n.730G>T
NM_001330347.1:c.434G>T NP_001317276.1:p.Ser145Ile
XM_005274008.3:c.-35G>T XP_005274065.1:n.-35G>T
XM_006718842.3:c.434G>T XP_006718905.1:p.Ser145Ile
XM_011542837.2:c.434G>T XP_011541139.1:p.Ser145Ile
XM_017017772.1:c.434G>T XP_016873261.1:p.Ser145Ile
XR_947828.2:n.730G>T
NM_001330347.2:c.434G>T NP_001317276.1:p.Ser145Ile
NM_005590.4:c.434G>T NP_005581.2:p.Ser145Ile
NM_005591.4:c.434G>T MANE Select NP_005582.1:p.Ser145Ile