Canonical Allele Identifier: CA351309
Gene: MRE11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94486070C>A , CM000673.2:g.94486070C>A GRCh38
NC_000011.9:g.94219236C>A , CM000673.1:g.94219236C>A GRCh37
NC_000011.8:g.93858884C>A NCBI36
NG_007261.1:g.12805G>T , LRG_85:g.12805G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000323929.8:c.168G>T MANE Select ENSP00000325863.4:p.Leu56Phe
ENST00000323929.7:c.168G>T ENSP00000325863.3:p.Leu56Phe
ENST00000323977.7:c.168G>T ENSP00000326094.3:p.Leu56Phe
ENST00000393241.8:c.168G>T ENSP00000376933.4:p.Leu56Phe
ENST00000407439.7:c.177G>T ENSP00000385614.3:p.Leu59Phe
ENST00000536144.1:n.403G>T
ENST00000536754.5:c.168G>T ENSP00000439511.1:p.Leu56Phe
ENST00000538923.1:c.168G>T ENSP00000442809.1:p.Leu56Phe
ENST00000540013.5:c.168G>T ENSP00000440986.1:p.Leu56Phe
ENST00000541157.5:n.332G>T
NM_005590.3:c.168G>T NP_005581.2:p.Leu56Phe
NM_005591.3:c.168G>T , LRG_85t1:c.168G>T NP_005582.1:p.Leu56Phe
XM_006718842.2:c.168G>T XP_006718905.1:p.Leu56Phe
XM_011542837.1:c.168G>T XP_011541139.1:p.Leu56Phe
XR_947828.1:n.464G>T
NM_001330347.1:c.168G>T NP_001317276.1:p.Leu56Phe
XM_005274008.3:c.-297G>T XP_005274065.1:n.-297G>T
XM_006718842.3:c.168G>T XP_006718905.1:p.Leu56Phe
XM_011542837.2:c.168G>T XP_011541139.1:p.Leu56Phe
XM_017017772.1:c.168G>T XP_016873261.1:p.Leu56Phe
XR_947828.2:n.464G>T
NM_001330347.2:c.168G>T NP_001317276.1:p.Leu56Phe
NM_005590.4:c.168G>T NP_005581.2:p.Leu56Phe
NM_005591.4:c.168G>T MANE Select NP_005582.1:p.Leu56Phe