Canonical Allele Identifier: CA1992441579
Gene: MRE11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94445659C= , CM000673.2:g.94445659C= GRCh38
NC_000011.9:g.94178825C= , CM000673.1:g.94178825C= GRCh37
NC_000011.8:g.93818473C= NCBI36
NG_007261.1:g.53216G= , LRG_85:g.53216G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323929.8:c.1867+151G= MANE Select ENSP00000325863.4:n.1867+151G=
ENST00000323929.7:c.1867+151G= ENSP00000325863.3:n.1867+151G=
ENST00000323977.7:c.1783+1560G= ENSP00000326094.3:n.1783+1560G=
ENST00000393241.8:c.1864+151G= ENSP00000376933.4:n.1864+151G=
ENST00000407439.7:c.1876+151G= ENSP00000385614.3:n.1876+151G=
NM_005590.3:c.1783+1560G= NP_005581.2:n.1783+1560G=
NM_005591.3:c.1867+151G= , LRG_85t1:c.1867+151G= NP_005582.1:n.1867+151G=
XM_005274008.2:c.1399+151G= XP_005274065.1:n.1399+151G=
XM_006718842.2:c.1864+151G= XP_006718905.1:n.1864+151G=
XM_011542837.1:c.1867+151G= XP_011541139.1:n.1867+151G=
XR_947828.1:n.2163+151G=
NM_001330347.1:c.1864+151G= NP_001317276.1:n.1864+151G=
XM_005274008.3:c.1399+151G= XP_005274065.1:n.1399+151G=
XM_006718842.3:c.1864+151G= XP_006718905.1:n.1864+151G=
XM_011542837.2:c.1867+151G= XP_011541139.1:n.1867+151G=
XM_017017772.1:c.1867+151G= XP_016873261.1:n.1867+151G=
XR_947828.2:n.2163+151G=
NM_001330347.2:c.1864+151G= NP_001317276.1:n.1864+151G=
NM_005590.4:c.1783+1560G= NP_005581.2:n.1783+1560G=
NM_005591.4:c.1867+151G= MANE Select NP_005582.1:n.1867+151G=