Canonical Allele Identifier: CA1630855260

Gene: MRE11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94417624T= , CM000673.2:g.94417624T=	GRCh38
NC_000011.9:g.94150790T= , CM000673.1:g.94150790T=	GRCh37
NC_000011.8:g.93790438T=	NCBI36
NG_007261.1:g.81251A= , LRG_85:g.81251A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323929.8:c.*2501A= MANE Select	ENSP00000325863.4:n.*2501A=
ENST00000323929.7:c.*2501A=	ENSP00000325863.3:n.*2501A=
NM_005590.3:c.*2501A=	NP_005581.2:n.*2501A=
NM_005591.3:c.*2501A= , LRG_85t1:c.*2501A=	NP_005582.1:n.*2501A=
XR_947828.1:n.4747+177A=
NM_001330347.1:c.*2501A=	NP_001317276.1:n.*2501A=
XM_005274008.3:c.*2501A=	XP_005274065.1:n.*2501A=
XM_006718842.3:c.*2501A=	XP_006718905.1:n.*2501A=
XM_011542837.2:c.*2501A=	XP_011541139.1:n.*2501A=
XM_017017772.1:c.*2501A=	XP_016873261.1:n.*2501A=
XR_947828.2:n.4747+177A=
NM_001330347.2:c.*2501A=	NP_001317276.1:n.*2501A=
NM_005590.4:c.*2501A=	NP_005581.2:n.*2501A=
NM_005591.4:c.*2501A= MANE Select	NP_005582.1:n.*2501A=