Canonical Allele Identifier: CA1992441732
Gene: MRE11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94445770T= , CM000673.2:g.94445770T= GRCh38
NC_000011.9:g.94178936T= , CM000673.1:g.94178936T= GRCh37
NC_000011.8:g.93818584T= NCBI36
NG_007261.1:g.53105A= , LRG_85:g.53105A=

Transcript Alleles

HGVS Amino-acid change
ENST00000323929.8:c.1867+40A= MANE Select ENSP00000325863.4:n.1867+40A=
ENST00000323929.7:c.1867+40A= ENSP00000325863.3:n.1867+40A=
ENST00000323977.7:c.1783+1449A= ENSP00000326094.3:n.1783+1449A=
ENST00000393241.8:c.1864+40A= ENSP00000376933.4:n.1864+40A=
ENST00000407439.7:c.1876+40A= ENSP00000385614.3:n.1876+40A=
ENST00000535120.1:n.203A=
NM_005590.3:c.1783+1449A= NP_005581.2:n.1783+1449A=
NM_005591.3:c.1867+40A= , LRG_85t1:c.1867+40A= NP_005582.1:n.1867+40A=
XM_005274008.2:c.1399+40A= XP_005274065.1:n.1399+40A=
XM_006718842.2:c.1864+40A= XP_006718905.1:n.1864+40A=
XM_011542837.1:c.1867+40A= XP_011541139.1:n.1867+40A=
XR_947828.1:n.2163+40A=
NM_001330347.1:c.1864+40A= NP_001317276.1:n.1864+40A=
XM_005274008.3:c.1399+40A= XP_005274065.1:n.1399+40A=
XM_006718842.3:c.1864+40A= XP_006718905.1:n.1864+40A=
XM_011542837.2:c.1867+40A= XP_011541139.1:n.1867+40A=
XM_017017772.1:c.1867+40A= XP_016873261.1:n.1867+40A=
XR_947828.2:n.2163+40A=
NM_001330347.2:c.1864+40A= NP_001317276.1:n.1864+40A=
NM_005590.4:c.1783+1449A= NP_005581.2:n.1783+1449A=
NM_005591.4:c.1867+40A= MANE Select NP_005582.1:n.1867+40A=