Canonical Allele Identifier: CA1992448295
Gene: MRE11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94435836G= , CM000673.2:g.94435836G= GRCh38
NC_000011.9:g.94169002G= , CM000673.1:g.94169002G= GRCh37
NC_000011.8:g.93808650G= NCBI36
NG_007261.1:g.63039C= , LRG_85:g.63039C=

Transcript Alleles

HGVS Amino-acid change
ENST00000323929.8:c.1990C= MANE Select ENSP00000325863.4:p.Gln664=
ENST00000323929.7:c.1990C= ENSP00000325863.3:p.Gln664=
ENST00000323977.7:c.1906C= ENSP00000326094.3:p.Gln636=
ENST00000393241.8:c.1987C= ENSP00000376933.4:p.Gln663=
ENST00000407439.7:c.1999C= ENSP00000385614.3:p.Gln667=
NM_005590.3:c.1906C= NP_005581.2:p.Gln636=
NM_005591.3:c.1990C= , LRG_85t1:c.1990C= NP_005582.1:p.Gln664=
XM_005274008.2:c.1522C= XP_005274065.1:p.Gln508=
XM_006718842.2:c.1987C= XP_006718905.1:p.Gln663=
XM_011542837.1:c.1990C= XP_011541139.1:p.Gln664=
XR_947828.1:n.2286C=
NM_001330347.1:c.1987C= NP_001317276.1:p.Gln663=
XM_005274008.3:c.1522C= XP_005274065.1:p.Gln508=
XM_006718842.3:c.1987C= XP_006718905.1:p.Gln663=
XM_011542837.2:c.1990C= XP_011541139.1:p.Gln664=
XM_017017772.1:c.1990C= XP_016873261.1:p.Gln664=
XR_947828.2:n.2286C=
NM_001330347.2:c.1987C= NP_001317276.1:p.Gln663=
NM_005590.4:c.1906C= NP_005581.2:p.Gln636=
NM_005591.4:c.1990C= MANE Select NP_005582.1:p.Gln664=