Canonical Allele Identifier: CA1992433110

Gene: MRE11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94476303C= , CM000673.2:g.94476303C=	GRCh38
NC_000011.9:g.94209469C= , CM000673.1:g.94209469C=	GRCh37
NC_000011.8:g.93849117C=	NCBI36
NG_007261.1:g.22572G= , LRG_85:g.22572G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323929.8:c.645G= MANE Select	ENSP00000325863.4:p.Val215=
ENST00000323929.7:c.645G=	ENSP00000325863.3:p.Val215=
ENST00000323977.7:c.645G=	ENSP00000326094.3:p.Val215=
ENST00000393241.8:c.645G=	ENSP00000376933.4:p.Val215=
ENST00000407439.7:c.654G=	ENSP00000385614.3:p.Val218=
ENST00000540013.5:c.645G=	ENSP00000440986.1:p.Val215=
NM_005590.3:c.645G=	NP_005581.2:p.Val215=
NM_005591.3:c.645G= , LRG_85t1:c.645G=	NP_005582.1:p.Val215=
XM_005274008.2:c.177G=	XP_005274065.1:p.Val59=
XM_006718842.2:c.645G=	XP_006718905.1:p.Val215=
XM_011542837.1:c.645G=	XP_011541139.1:p.Val215=
XR_947828.1:n.941G=
NM_001330347.1:c.645G=	NP_001317276.1:p.Val215=
XM_005274008.3:c.177G=	XP_005274065.1:p.Val59=
XM_006718842.3:c.645G=	XP_006718905.1:p.Val215=
XM_011542837.2:c.645G=	XP_011541139.1:p.Val215=
XM_017017772.1:c.645G=	XP_016873261.1:p.Val215=
XR_947828.2:n.941G=
NM_001330347.2:c.645G=	NP_001317276.1:p.Val215=
NM_005590.4:c.645G=	NP_005581.2:p.Val215=
NM_005591.4:c.645G= MANE Select	NP_005582.1:p.Val215=