Canonical Allele Identifier: CA15681832
Gene: MRE11 HGNC NCBI

Linked Data

dbSNP Id: rs2508784

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94488198A>G , CM000673.2:g.94488198A>G GRCh38
NC_000011.9:g.94221364A>G , CM000673.1:g.94221364A>G GRCh37
NC_000011.8:g.93861012A>G NCBI36
NG_007261.1:g.10677T>C , LRG_85:g.10677T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000323929.8:c.154-2114T>C MANE Select ENSP00000325863.4:n.154-2114T>C
ENST00000323929.7:c.154-2114T>C ENSP00000325863.3:n.154-2114T>C
ENST00000323977.7:c.154-2114T>C ENSP00000326094.3:n.154-2114T>C
ENST00000393241.8:c.154-2114T>C ENSP00000376933.4:n.154-2114T>C
ENST00000407439.7:c.163-2114T>C ENSP00000385614.3:n.163-2114T>C
ENST00000536144.1:n.389-2114T>C
ENST00000536754.5:c.154-2114T>C ENSP00000439511.1:n.154-2114T>C
ENST00000538923.1:c.154-2114T>C ENSP00000442809.1:n.154-2114T>C
ENST00000540013.5:c.154-2114T>C ENSP00000440986.1:n.154-2114T>C
ENST00000541157.5:n.318-2114T>C
NM_005590.3:c.154-2114T>C NP_005581.2:n.154-2114T>C
NM_005591.3:c.154-2114T>C , LRG_85t1:c.154-2114T>C NP_005582.1:n.154-2114T>C
XM_006718842.2:c.154-2114T>C XP_006718905.1:n.154-2114T>C
XM_011542837.1:c.154-2114T>C XP_011541139.1:n.154-2114T>C
XR_947828.1:n.450-2114T>C
NM_001330347.1:c.154-2114T>C NP_001317276.1:n.154-2114T>C
XM_005274008.3:c.-311-2114T>C XP_005274065.1:n.-311-2114T>C
XM_006718842.3:c.154-2114T>C XP_006718905.1:n.154-2114T>C
XM_011542837.2:c.154-2114T>C XP_011541139.1:n.154-2114T>C
XM_017017772.1:c.154-2114T>C XP_016873261.1:n.154-2114T>C
XR_947828.2:n.450-2114T>C
NM_001330347.2:c.154-2114T>C NP_001317276.1:n.154-2114T>C
NM_005590.4:c.154-2114T>C NP_005581.2:n.154-2114T>C
NM_005591.4:c.154-2114T>C MANE Select NP_005582.1:n.154-2114T>C