Canonical Allele Identifier: CA226544748

Gene: MRE11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94490975G>C , CM000673.2:g.94490975G>C	GRCh38
NC_000011.9:g.94224141G>C , CM000673.1:g.94224141G>C	GRCh37
NC_000011.8:g.93863789G>C	NCBI36
NG_007261.1:g.7900C>G , LRG_85:g.7900C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_005591.4:c.21-10C>G MANE Select	NP_005582.1:n.21-10C>G
ENST00000323929.8:c.21-10C>G MANE Select	ENSP00000325863.4:n.21-10C>G
NM_001330347.1:c.21-10C>G	NP_001317276.1:n.21-10C>G
NM_001330347.2:c.21-10C>G	NP_001317276.1:n.21-10C>G
NM_005590.3:c.21-10C>G	NP_005581.2:n.21-10C>G
NM_005590.4:c.21-10C>G	NP_005581.2:n.21-10C>G
NM_005591.3:c.21-10C>G , LRG_85t1:c.21-10C>G	NP_005582.1:n.21-10C>G
ENST00000323929.7:c.21-10C>G	ENSP00000325863.3:n.21-10C>G
ENST00000323977.7:c.21-10C>G	ENSP00000326094.3:n.21-10C>G
ENST00000393241.8:c.21-10C>G	ENSP00000376933.4:n.21-10C>G
ENST00000407439.7:c.30-10C>G	ENSP00000385614.3:n.30-10C>G
ENST00000536144.1:n.256-10C>G
ENST00000536754.5:c.21-10C>G	ENSP00000439511.1:n.21-10C>G
ENST00000538923.1:c.21-10C>G	ENSP00000442809.1:n.21-10C>G
ENST00000540013.5:c.21-10C>G	ENSP00000440986.1:n.21-10C>G
ENST00000541157.5:n.185-10C>G
XM_006718842.2:c.21-10C>G	XP_006718905.1:n.21-10C>G
XM_006718842.3:c.21-10C>G	XP_006718905.1:n.21-10C>G
XM_011542837.1:c.21-10C>G	XP_011541139.1:n.21-10C>G
XM_011542837.2:c.21-10C>G	XP_011541139.1:n.21-10C>G
XM_017017772.1:c.21-10C>G	XP_016873261.1:n.21-10C>G
XR_947828.1:n.317-10C>G
XR_947828.2:n.317-10C>G