Canonical Allele Identifier: CA1992441805

Gene: MRE11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94445810C= , CM000673.2:g.94445810C=	GRCh38
NC_000011.9:g.94178976C= , CM000673.1:g.94178976C=	GRCh37
NC_000011.8:g.93818624C=	NCBI36
NG_007261.1:g.53065G= , LRG_85:g.53065G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000323929.8:c.1867G= MANE Select	ENSP00000325863.4:p.Ala623=
ENST00000323929.7:c.1867G=	ENSP00000325863.3:p.Ala623=
ENST00000323977.7:c.1783+1409G=	ENSP00000326094.3:n.1783+1409G=
ENST00000393241.8:c.1864G=	ENSP00000376933.4:p.Ala622=
ENST00000407439.7:c.1876G=	ENSP00000385614.3:p.Ala626=
ENST00000535120.1:n.163G=
NM_005590.3:c.1783+1409G=	NP_005581.2:n.1783+1409G=
NM_005591.3:c.1867G= , LRG_85t1:c.1867G=	NP_005582.1:p.Ala623=
XM_005274008.2:c.1399G=	XP_005274065.1:p.Ala467=
XM_006718842.2:c.1864G=	XP_006718905.1:p.Ala622=
XM_011542837.1:c.1867G=	XP_011541139.1:p.Ala623=
XR_947828.1:n.2163G=
NM_001330347.1:c.1864G=	NP_001317276.1:p.Ala622=
XM_005274008.3:c.1399G=	XP_005274065.1:p.Ala467=
XM_006718842.3:c.1864G=	XP_006718905.1:p.Ala622=
XM_011542837.2:c.1867G=	XP_011541139.1:p.Ala623=
XM_017017772.1:c.1867G=	XP_016873261.1:p.Ala623=
XR_947828.2:n.2163G=
NM_001330347.2:c.1864G=	NP_001317276.1:p.Ala622=
NM_005590.4:c.1783+1409G=	NP_005581.2:n.1783+1409G=
NM_005591.4:c.1867G= MANE Select	NP_005582.1:p.Ala623=