Canonical Allele Identifier: CA1992441758

Gene: MRE11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94445788A= , CM000673.2:g.94445788A=	GRCh38
NC_000011.9:g.94178954A= , CM000673.1:g.94178954A=	GRCh37
NC_000011.8:g.93818602A=	NCBI36
NG_007261.1:g.53087T= , LRG_85:g.53087T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323929.8:c.1867+22T= MANE Select	ENSP00000325863.4:n.1867+22T=
ENST00000323929.7:c.1867+22T=	ENSP00000325863.3:n.1867+22T=
ENST00000323977.7:c.1783+1431T=	ENSP00000326094.3:n.1783+1431T=
ENST00000393241.8:c.1864+22T=	ENSP00000376933.4:n.1864+22T=
ENST00000407439.7:c.1876+22T=	ENSP00000385614.3:n.1876+22T=
ENST00000535120.1:n.185T=
NM_005590.3:c.1783+1431T=	NP_005581.2:n.1783+1431T=
NM_005591.3:c.1867+22T= , LRG_85t1:c.1867+22T=	NP_005582.1:n.1867+22T=
XM_005274008.2:c.1399+22T=	XP_005274065.1:n.1399+22T=
XM_006718842.2:c.1864+22T=	XP_006718905.1:n.1864+22T=
XM_011542837.1:c.1867+22T=	XP_011541139.1:n.1867+22T=
XR_947828.1:n.2163+22T=
NM_001330347.1:c.1864+22T=	NP_001317276.1:n.1864+22T=
XM_005274008.3:c.1399+22T=	XP_005274065.1:n.1399+22T=
XM_006718842.3:c.1864+22T=	XP_006718905.1:n.1864+22T=
XM_011542837.2:c.1867+22T=	XP_011541139.1:n.1867+22T=
XM_017017772.1:c.1867+22T=	XP_016873261.1:n.1867+22T=
XR_947828.2:n.2163+22T=
NM_001330347.2:c.1864+22T=	NP_001317276.1:n.1864+22T=
NM_005590.4:c.1783+1431T=	NP_005581.2:n.1783+1431T=
NM_005591.4:c.1867+22T= MANE Select	NP_005582.1:n.1867+22T=