Canonical Allele Identifier: CA1139662137

Gene: MRE11 ANKRD49

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94493780T>C , CM000673.2:g.94493780T>C	GRCh38
NC_000011.9:g.94226946T>C , CM000673.1:g.94226946T>C	GRCh37
NC_000011.8:g.93866594T>C	NCBI36
NG_007261.1:g.5095A>G , LRG_85:g.5095A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_005591.4:c.-106+11A>G (MRE11) MANE Select	NP_005582.1:n.-106+11A>G
ENST00000323929.8:c.-106+11A>G (MRE11) MANE Select	ENSP00000325863.4:n.-106+11A>G
NM_001330347.1:c.-106+11A>G (MRE11)	NP_001317276.1:n.-106+11A>G
NM_001330347.2:c.-106+11A>G (MRE11)	NP_001317276.1:n.-106+11A>G
NM_005590.3:c.-202A>G (MRE11)	NP_005581.2:n.-202A>G
NM_005590.4:c.-202A>G (MRE11)	NP_005581.2:n.-202A>G
NM_005591.3:c.-106+11A>G , LRG_85t1:c.-106+11A>G (MRE11)	NP_005582.1:n.-106+11A>G
ENST00000323929.7:c.-106+11A>G (MRE11)	ENSP00000325863.3:n.-106+11A>G
ENST00000323977.7:c.-202A>G (MRE11)	ENSP00000326094.3:n.-202A>G
ENST00000393241.8:c.-165A>G (MRE11)	ENSP00000376933.4:n.-165A>G
ENST00000407439.7:c.-237+11A>G (MRE11)	ENSP00000385614.3:n.-237+11A>G
ENST00000536144.1:n.34A>G (MRE11)
ENST00000536754.5:c.-97+11A>G (MRE11)	ENSP00000439511.1:n.-97+11A>G
ENST00000538923.1:c.-193A>G (MRE11)	ENSP00000442809.1:n.-193A>G
ENST00000540013.5:c.-106+11A>G (MRE11)	ENSP00000440986.1:n.-106+11A>G
ENST00000541157.5:n.59+11A>G (MRE11)
ENST00000544612.5:c.-346T>C (ANKRD49)	ENSP00000440396.1:n.-346T>C
XM_006718842.2:c.-202A>G (MRE11)	XP_006718905.1:n.-202A>G
XM_006718842.3:c.-202A>G (MRE11)	XP_006718905.1:n.-202A>G
XM_011542837.1:c.-105-874A>G (MRE11)	XP_011541139.1:n.-105-874A>G
XM_011542837.2:c.-105-874A>G (MRE11)	XP_011541139.1:n.-105-874A>G
XM_017017772.1:c.-202A>G (MRE11)	XP_016873261.1:n.-202A>G
XR_947828.1:n.95A>G (MRE11)
XR_947828.2:n.95A>G (MRE11)