Canonical Allele Identifier: CA1992468776

Gene: MRE11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94464168A= , CM000673.2:g.94464168A=	GRCh38
NC_000011.9:g.94197334A= , CM000673.1:g.94197334A=	GRCh37
NC_000011.8:g.93836982A=	NCBI36
NG_007261.1:g.34707T= , LRG_85:g.34707T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323929.8:c.1170T= MANE Select	ENSP00000325863.4:p.Ala390=
ENST00000323929.7:c.1170T=	ENSP00000325863.3:p.Ala390=
ENST00000323977.7:c.1170T=	ENSP00000326094.3:p.Ala390=
ENST00000393241.8:c.1170T=	ENSP00000376933.4:p.Ala390=
ENST00000407439.7:c.1179T=	ENSP00000385614.3:p.Ala393=
NM_005590.3:c.1170T=	NP_005581.2:p.Ala390=
NM_005591.3:c.1170T= , LRG_85t1:c.1170T=	NP_005582.1:p.Ala390=
XM_005274008.2:c.702T=	XP_005274065.1:p.Ala234=
XM_006718842.2:c.1170T=	XP_006718905.1:p.Ala390=
XM_011542837.1:c.1170T=	XP_011541139.1:p.Ala390=
XR_947828.1:n.1466T=
NM_001330347.1:c.1170T=	NP_001317276.1:p.Ala390=
XM_005274008.3:c.702T=	XP_005274065.1:p.Ala234=
XM_006718842.3:c.1170T=	XP_006718905.1:p.Ala390=
XM_011542837.2:c.1170T=	XP_011541139.1:p.Ala390=
XM_017017772.1:c.1170T=	XP_016873261.1:p.Ala390=
XR_947828.2:n.1466T=
NM_001330347.2:c.1170T=	NP_001317276.1:p.Ala390=
NM_005590.4:c.1170T=	NP_005581.2:p.Ala390=
NM_005591.4:c.1170T= MANE Select	NP_005582.1:p.Ala390=