Canonical Allele Identifier: CA1992438815

Gene: MRE11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94479726T= , CM000673.2:g.94479726T=	GRCh38
NC_000011.9:g.94212892T= , CM000673.1:g.94212892T=	GRCh37
NC_000011.8:g.93852540T=	NCBI36
NG_007261.1:g.19149A= , LRG_85:g.19149A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000323929.8:c.350A= MANE Select	ENSP00000325863.4:p.Asn117=
ENST00000323929.7:c.350A=	ENSP00000325863.3:p.Asn117=
ENST00000323977.7:c.350A=	ENSP00000326094.3:p.Asn117=
ENST00000393241.8:c.350A=	ENSP00000376933.4:p.Asn117=
ENST00000407439.7:c.359A=	ENSP00000385614.3:p.Asn120=
ENST00000536754.5:c.350A=	ENSP00000439511.1:p.Asn117=
ENST00000540013.5:c.350A=	ENSP00000440986.1:p.Asn117=
ENST00000541157.5:n.479-850A=
NM_005590.3:c.350A=	NP_005581.2:p.Asn117=
NM_005591.3:c.350A= , LRG_85t1:c.350A=	NP_005582.1:p.Asn117=
XM_005274008.2:c.-119A=	XP_005274065.1:n.-119A=
XM_006718842.2:c.350A=	XP_006718905.1:p.Asn117=
XM_011542837.1:c.350A=	XP_011541139.1:p.Asn117=
XR_947828.1:n.646A=
NM_001330347.1:c.350A=	NP_001317276.1:p.Asn117=
XM_005274008.3:c.-119A=	XP_005274065.1:n.-119A=
XM_006718842.3:c.350A=	XP_006718905.1:p.Asn117=
XM_011542837.2:c.350A=	XP_011541139.1:p.Asn117=
XM_017017772.1:c.350A=	XP_016873261.1:p.Asn117=
XR_947828.2:n.646A=
NM_001330347.2:c.350A=	NP_001317276.1:p.Asn117=
NM_005590.4:c.350A=	NP_005581.2:p.Asn117=
NM_005591.4:c.350A= MANE Select	NP_005582.1:p.Asn117=