Canonical Allele Identifier: CA1992442086
Gene: MRE11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94445876T= , CM000673.2:g.94445876T= GRCh38
NC_000011.9:g.94179042T= , CM000673.1:g.94179042T= GRCh37
NC_000011.8:g.93818690T= NCBI36
NG_007261.1:g.52999A= , LRG_85:g.52999A=

Transcript Alleles

HGVS Amino-acid change
ENST00000323929.8:c.1801A= MANE Select ENSP00000325863.4:p.Thr601=
ENST00000323929.7:c.1801A= ENSP00000325863.3:p.Thr601=
ENST00000323977.7:c.1783+1343A= ENSP00000326094.3:n.1783+1343A=
ENST00000393241.8:c.1798A= ENSP00000376933.4:p.Thr600=
ENST00000407439.7:c.1810A= ENSP00000385614.3:p.Thr604=
ENST00000535120.1:n.97A=
NM_005590.3:c.1783+1343A= NP_005581.2:n.1783+1343A=
NM_005591.3:c.1801A= , LRG_85t1:c.1801A= NP_005582.1:p.Thr601=
XM_005274008.2:c.1333A= XP_005274065.1:p.Thr445=
XM_006718842.2:c.1798A= XP_006718905.1:p.Thr600=
XM_011542837.1:c.1801A= XP_011541139.1:p.Thr601=
XR_947828.1:n.2097A=
NM_001330347.1:c.1798A= NP_001317276.1:p.Thr600=
XM_005274008.3:c.1333A= XP_005274065.1:p.Thr445=
XM_006718842.3:c.1798A= XP_006718905.1:p.Thr600=
XM_011542837.2:c.1801A= XP_011541139.1:p.Thr601=
XM_017017772.1:c.1801A= XP_016873261.1:p.Thr601=
XR_947828.2:n.2097A=
NM_001330347.2:c.1798A= NP_001317276.1:p.Thr600=
NM_005590.4:c.1783+1343A= NP_005581.2:n.1783+1343A=
NM_005591.4:c.1801A= MANE Select NP_005582.1:p.Thr601=