Canonical Allele Identifier: CA1992440596

Gene: MRE11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94480739G= , CM000673.2:g.94480739G=	GRCh38
NC_000011.9:g.94213905G= , CM000673.1:g.94213905G=	GRCh37
NC_000011.8:g.93853553G=	NCBI36
NG_007261.1:g.18136C= , LRG_85:g.18136C=

Transcript Alleles

HGVS	Amino-acid Change
NM_005591.4:c.315-978C= MANE Select	NP_005582.1:n.315-978C=
ENST00000323929.8:c.315-978C= MANE Select	ENSP00000325863.4:n.315-978C=
NM_001330347.1:c.315-978C=	NP_001317276.1:n.315-978C=
NM_001330347.2:c.315-978C=	NP_001317276.1:n.315-978C=
NM_005590.3:c.315-978C=	NP_005581.2:n.315-978C=
NM_005590.4:c.315-978C=	NP_005581.2:n.315-978C=
NM_005591.3:c.315-978C= , LRG_85t1:c.315-978C=	NP_005582.1:n.315-978C=
ENST00000323929.7:c.315-978C=	ENSP00000325863.3:n.315-978C=
ENST00000323977.7:c.315-978C=	ENSP00000326094.3:n.315-978C=
ENST00000393241.8:c.315-978C=	ENSP00000376933.4:n.315-978C=
ENST00000407439.7:c.324-978C=	ENSP00000385614.3:n.324-978C=
ENST00000536754.5:c.315-978C=	ENSP00000439511.1:n.315-978C=
ENST00000538923.1:c.315-978C=	ENSP00000442809.1:n.315-978C=
ENST00000540013.5:c.315-978C=	ENSP00000440986.1:n.315-978C=
ENST00000541157.5:n.479-1863C=
XM_005274008.2:c.-154-978C=	XP_005274065.1:n.-154-978C=
XM_005274008.3:c.-154-978C=	XP_005274065.1:n.-154-978C=
XM_006718842.2:c.315-978C=	XP_006718905.1:n.315-978C=
XM_006718842.3:c.315-978C=	XP_006718905.1:n.315-978C=
XM_011542837.1:c.315-978C=	XP_011541139.1:n.315-978C=
XM_011542837.2:c.315-978C=	XP_011541139.1:n.315-978C=
XM_017017772.1:c.315-978C=	XP_016873261.1:n.315-978C=
XR_947828.1:n.611-978C=
XR_947828.2:n.611-978C=