Canonical Allele Identifier: CA1992442179
Gene: MRE11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94445885C= , CM000673.2:g.94445885C= GRCh38
NC_000011.9:g.94179051C= , CM000673.1:g.94179051C= GRCh37
NC_000011.8:g.93818699C= NCBI36
NG_007261.1:g.52990G= , LRG_85:g.52990G=

Transcript Alleles

HGVS Amino-acid change
ENST00000323929.8:c.1792G= MANE Select ENSP00000325863.4:p.Gly598=
ENST00000323929.7:c.1792G= ENSP00000325863.3:p.Gly598=
ENST00000323977.7:c.1783+1334G= ENSP00000326094.3:n.1783+1334G=
ENST00000393241.8:c.1789G= ENSP00000376933.4:p.Gly597=
ENST00000407439.7:c.1801G= ENSP00000385614.3:p.Gly601=
ENST00000535120.1:n.88G=
NM_005590.3:c.1783+1334G= NP_005581.2:n.1783+1334G=
NM_005591.3:c.1792G= , LRG_85t1:c.1792G= NP_005582.1:p.Gly598=
XM_005274008.2:c.1324G= XP_005274065.1:p.Gly442=
XM_006718842.2:c.1789G= XP_006718905.1:p.Gly597=
XM_011542837.1:c.1792G= XP_011541139.1:p.Gly598=
XR_947828.1:n.2088G=
NM_001330347.1:c.1789G= NP_001317276.1:p.Gly597=
XM_005274008.3:c.1324G= XP_005274065.1:p.Gly442=
XM_006718842.3:c.1789G= XP_006718905.1:p.Gly597=
XM_011542837.2:c.1792G= XP_011541139.1:p.Gly598=
XM_017017772.1:c.1792G= XP_016873261.1:p.Gly598=
XR_947828.2:n.2088G=
NM_001330347.2:c.1789G= NP_001317276.1:p.Gly597=
NM_005590.4:c.1783+1334G= NP_005581.2:n.1783+1334G=
NM_005591.4:c.1792G= MANE Select NP_005582.1:p.Gly598=