Canonical Allele Identifier: CA1992426161
Gene: MRE11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94435878C= , CM000673.2:g.94435878C= GRCh38
NC_000011.9:g.94169044C= , CM000673.1:g.94169044C= GRCh37
NC_000011.8:g.93808692C= NCBI36
NG_007261.1:g.62997G= , LRG_85:g.62997G=

Transcript Alleles

HGVS Amino-acid change
ENST00000323929.8:c.1948G= MANE Select ENSP00000325863.4:p.Asp650=
ENST00000323929.7:c.1948G= ENSP00000325863.3:p.Asp650=
ENST00000323977.7:c.1864G= ENSP00000326094.3:p.Asp622=
ENST00000393241.8:c.1945G= ENSP00000376933.4:p.Asp649=
ENST00000407439.7:c.1957G= ENSP00000385614.3:p.Asp653=
NM_005590.3:c.1864G= NP_005581.2:p.Asp622=
NM_005591.3:c.1948G= , LRG_85t1:c.1948G= NP_005582.1:p.Asp650=
XM_005274008.2:c.1480G= XP_005274065.1:p.Asp494=
XM_006718842.2:c.1945G= XP_006718905.1:p.Asp649=
XM_011542837.1:c.1948G= XP_011541139.1:p.Asp650=
XR_947828.1:n.2244G=
NM_001330347.1:c.1945G= NP_001317276.1:p.Asp649=
XM_005274008.3:c.1480G= XP_005274065.1:p.Asp494=
XM_006718842.3:c.1945G= XP_006718905.1:p.Asp649=
XM_011542837.2:c.1948G= XP_011541139.1:p.Asp650=
XM_017017772.1:c.1948G= XP_016873261.1:p.Asp650=
XR_947828.2:n.2244G=
NM_001330347.2:c.1945G= NP_001317276.1:p.Asp649=
NM_005590.4:c.1864G= NP_005581.2:p.Asp622=
NM_005591.4:c.1948G= MANE Select NP_005582.1:p.Asp650=