Canonical Allele Identifier: CA1992442984

Gene: MRE11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94446326_94446328delinsGAA , CM000673.2:g.94446326_94446328delinsGAA	GRCh38
NC_000011.9:g.94179492_94179494delinsGAA , CM000673.1:g.94179492_94179494delinsGAA	GRCh37
NC_000011.8:g.93819140_93819142delinsGAA	NCBI36
NG_007261.1:g.52547_52549delinsTTC , LRG_85:g.52547_52549delinsTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323929.8:c.1784-435_1784-433delinsTTC MANE Select	ENSP00000325863.4:n.1784-435_1784-433delinsTTC
ENST00000323929.7:c.1784-435_1784-433delinsTTC	ENSP00000325863.3:n.1784-435_1784-433delinsTTC
ENST00000323977.7:c.1783+891_1783+893delinsTTC	ENSP00000326094.3:n.1783+891_1783+893delinsTTC
ENST00000393241.8:c.1784-438_1784-436delinsTTC	ENSP00000376933.4:n.1784-438_1784-436delinsTTC
ENST00000407439.7:c.1793-435_1793-433delinsTTC	ENSP00000385614.3:n.1793-435_1793-433delinsTTC
ENST00000535120.1:n.83-438_83-436delinsTTC
NM_005590.3:c.1783+891_1783+893delinsTTC	NP_005581.2:n.1783+891_1783+893delinsTTC
NM_005591.3:c.1784-435_1784-433delinsTTC , LRG_85t1:c.1784-435_1784-433delinsTTC	NP_005582.1:n.1784-435_1784-433delinsTTC
XM_005274008.2:c.1316-435_1316-433delinsTTC	XP_005274065.1:n.1316-435_1316-433delinsTTC
XM_006718842.2:c.1784-438_1784-436delinsTTC	XP_006718905.1:n.1784-438_1784-436delinsTTC
XM_011542837.1:c.1784-435_1784-433delinsTTC	XP_011541139.1:n.1784-435_1784-433delinsTTC
XR_947828.1:n.2080-435_2080-433delinsTTC
NM_001330347.1:c.1784-438_1784-436delinsTTC	NP_001317276.1:n.1784-438_1784-436delinsTTC
XM_005274008.3:c.1316-435_1316-433delinsTTC	XP_005274065.1:n.1316-435_1316-433delinsTTC
XM_006718842.3:c.1784-438_1784-436delinsTTC	XP_006718905.1:n.1784-438_1784-436delinsTTC
XM_011542837.2:c.1784-435_1784-433delinsTTC	XP_011541139.1:n.1784-435_1784-433delinsTTC
XM_017017772.1:c.1784-435_1784-433delinsTTC	XP_016873261.1:n.1784-435_1784-433delinsTTC
XR_947828.2:n.2080-435_2080-433delinsTTC
NM_001330347.2:c.1784-438_1784-436delinsTTC	NP_001317276.1:n.1784-438_1784-436delinsTTC
NM_005590.4:c.1783+891_1783+893delinsTTC	NP_005581.2:n.1783+891_1783+893delinsTTC
NM_005591.4:c.1784-435_1784-433delinsTTC MANE Select	NP_005582.1:n.1784-435_1784-433delinsTTC