Canonical Allele Identifier: CA1992441835

Gene: MRE11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94445819T= , CM000673.2:g.94445819T=	GRCh38
NC_000011.9:g.94178985T= , CM000673.1:g.94178985T=	GRCh37
NC_000011.8:g.93818633T=	NCBI36
NG_007261.1:g.53056A= , LRG_85:g.53056A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000323929.8:c.1858A= MANE Select	ENSP00000325863.4:p.Ile620=
ENST00000323929.7:c.1858A=	ENSP00000325863.3:p.Ile620=
ENST00000323977.7:c.1783+1400A=	ENSP00000326094.3:n.1783+1400A=
ENST00000393241.8:c.1855A=	ENSP00000376933.4:p.Ile619=
ENST00000407439.7:c.1867A=	ENSP00000385614.3:p.Ile623=
ENST00000535120.1:n.154A=
NM_005590.3:c.1783+1400A=	NP_005581.2:n.1783+1400A=
NM_005591.3:c.1858A= , LRG_85t1:c.1858A=	NP_005582.1:p.Ile620=
XM_005274008.2:c.1390A=	XP_005274065.1:p.Ile464=
XM_006718842.2:c.1855A=	XP_006718905.1:p.Ile619=
XM_011542837.1:c.1858A=	XP_011541139.1:p.Ile620=
XR_947828.1:n.2154A=
NM_001330347.1:c.1855A=	NP_001317276.1:p.Ile619=
XM_005274008.3:c.1390A=	XP_005274065.1:p.Ile464=
XM_006718842.3:c.1855A=	XP_006718905.1:p.Ile619=
XM_011542837.2:c.1858A=	XP_011541139.1:p.Ile620=
XM_017017772.1:c.1858A=	XP_016873261.1:p.Ile620=
XR_947828.2:n.2154A=
NM_001330347.2:c.1855A=	NP_001317276.1:p.Ile619=
NM_005590.4:c.1783+1400A=	NP_005581.2:n.1783+1400A=
NM_005591.4:c.1858A= MANE Select	NP_005582.1:p.Ile620=