Canonical Allele Identifier: CA1992441858
Gene: MRE11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94445824A= , CM000673.2:g.94445824A= GRCh38
NC_000011.9:g.94178990A= , CM000673.1:g.94178990A= GRCh37
NC_000011.8:g.93818638A= NCBI36
NG_007261.1:g.53051T= , LRG_85:g.53051T=

Transcript Alleles

HGVS Amino-acid change
ENST00000323929.8:c.1853T= MANE Select ENSP00000325863.4:p.Met618=
ENST00000323929.7:c.1853T= ENSP00000325863.3:p.Met618=
ENST00000323977.7:c.1783+1395T= ENSP00000326094.3:n.1783+1395T=
ENST00000393241.8:c.1850T= ENSP00000376933.4:p.Met617=
ENST00000407439.7:c.1862T= ENSP00000385614.3:p.Met621=
ENST00000535120.1:n.149T=
NM_005590.3:c.1783+1395T= NP_005581.2:n.1783+1395T=
NM_005591.3:c.1853T= , LRG_85t1:c.1853T= NP_005582.1:p.Met618=
XM_005274008.2:c.1385T= XP_005274065.1:p.Met462=
XM_006718842.2:c.1850T= XP_006718905.1:p.Met617=
XM_011542837.1:c.1853T= XP_011541139.1:p.Met618=
XR_947828.1:n.2149T=
NM_001330347.1:c.1850T= NP_001317276.1:p.Met617=
XM_005274008.3:c.1385T= XP_005274065.1:p.Met462=
XM_006718842.3:c.1850T= XP_006718905.1:p.Met617=
XM_011542837.2:c.1853T= XP_011541139.1:p.Met618=
XM_017017772.1:c.1853T= XP_016873261.1:p.Met618=
XR_947828.2:n.2149T=
NM_001330347.2:c.1850T= NP_001317276.1:p.Met617=
NM_005590.4:c.1783+1395T= NP_005581.2:n.1783+1395T=
NM_005591.4:c.1853T= MANE Select NP_005582.1:p.Met618=