Canonical Allele Identifier: CA382366250
Gene: MRE11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94445819T>A , CM000673.2:g.94445819T>A GRCh38
NC_000011.9:g.94178985T>A , CM000673.1:g.94178985T>A GRCh37
NC_000011.8:g.93818633T>A NCBI36
NG_007261.1:g.53056A>T , LRG_85:g.53056A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000323929.8:c.1858A>T MANE Select ENSP00000325863.4:p.Ile620Phe
ENST00000323929.7:c.1858A>T ENSP00000325863.3:p.Ile620Phe
ENST00000323977.7:c.1783+1400A>T ENSP00000326094.3:n.1783+1400A>T
ENST00000393241.8:c.1855A>T ENSP00000376933.4:p.Ile619Phe
ENST00000407439.7:c.1867A>T ENSP00000385614.3:p.Ile623Phe
ENST00000535120.1:n.154A>T
NM_005590.3:c.1783+1400A>T NP_005581.2:n.1783+1400A>T
NM_005591.3:c.1858A>T , LRG_85t1:c.1858A>T NP_005582.1:p.Ile620Phe
XM_005274008.2:c.1390A>T XP_005274065.1:p.Ile464Phe
XM_006718842.2:c.1855A>T XP_006718905.1:p.Ile619Phe
XM_011542837.1:c.1858A>T XP_011541139.1:p.Ile620Phe
XR_947828.1:n.2154A>T
NM_001330347.1:c.1855A>T NP_001317276.1:p.Ile619Phe
XM_005274008.3:c.1390A>T XP_005274065.1:p.Ile464Phe
XM_006718842.3:c.1855A>T XP_006718905.1:p.Ile619Phe
XM_011542837.2:c.1858A>T XP_011541139.1:p.Ile620Phe
XM_017017772.1:c.1858A>T XP_016873261.1:p.Ile620Phe
XR_947828.2:n.2154A>T
NM_001330347.2:c.1855A>T NP_001317276.1:p.Ile619Phe
NM_005590.4:c.1783+1400A>T NP_005581.2:n.1783+1400A>T
NM_005591.4:c.1858A>T MANE Select NP_005582.1:p.Ile620Phe