Canonical Allele Identifier: CA1992426069
Gene: MRE11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94435846T= , CM000673.2:g.94435846T= GRCh38
NC_000011.9:g.94169012T= , CM000673.1:g.94169012T= GRCh37
NC_000011.8:g.93808660T= NCBI36
NG_007261.1:g.63029A= , LRG_85:g.63029A=

Transcript Alleles

HGVS Amino-acid change
ENST00000323929.8:c.1980A= MANE Select ENSP00000325863.4:p.Ser660=
ENST00000323929.7:c.1980A= ENSP00000325863.3:p.Ser660=
ENST00000323977.7:c.1896A= ENSP00000326094.3:p.Ser632=
ENST00000393241.8:c.1977A= ENSP00000376933.4:p.Ser659=
ENST00000407439.7:c.1989A= ENSP00000385614.3:p.Ser663=
NM_005590.3:c.1896A= NP_005581.2:p.Ser632=
NM_005591.3:c.1980A= , LRG_85t1:c.1980A= NP_005582.1:p.Ser660=
XM_005274008.2:c.1512A= XP_005274065.1:p.Ser504=
XM_006718842.2:c.1977A= XP_006718905.1:p.Ser659=
XM_011542837.1:c.1980A= XP_011541139.1:p.Ser660=
XR_947828.1:n.2276A=
NM_001330347.1:c.1977A= NP_001317276.1:p.Ser659=
XM_005274008.3:c.1512A= XP_005274065.1:p.Ser504=
XM_006718842.3:c.1977A= XP_006718905.1:p.Ser659=
XM_011542837.2:c.1980A= XP_011541139.1:p.Ser660=
XM_017017772.1:c.1980A= XP_016873261.1:p.Ser660=
XR_947828.2:n.2276A=
NM_001330347.2:c.1977A= NP_001317276.1:p.Ser659=
NM_005590.4:c.1896A= NP_005581.2:p.Ser632=
NM_005591.4:c.1980A= MANE Select NP_005582.1:p.Ser660=