Canonical Allele Identifier: CA1992442944

Gene: MRE11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94446312_94446315delinsCAGG , CM000673.2:g.94446312_94446315delinsCAGG	GRCh38
NC_000011.9:g.94179478_94179481delinsCAGG , CM000673.1:g.94179478_94179481delinsCAGG	GRCh37
NC_000011.8:g.93819126_93819129delinsCAGG	NCBI36
NG_007261.1:g.52560_52563delinsCCTG , LRG_85:g.52560_52563delinsCCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323929.8:c.1784-422_1784-419delinsCCTG MANE Select	ENSP00000325863.4:n.1784-422_1784-419delinsCCTG
ENST00000323929.7:c.1784-422_1784-419delinsCCTG	ENSP00000325863.3:n.1784-422_1784-419delinsCCTG
ENST00000323977.7:c.1783+904_1783+907delinsCCTG	ENSP00000326094.3:n.1783+904_1783+907delinsCCTG
ENST00000393241.8:c.1784-425_1784-422delinsCCTG	ENSP00000376933.4:n.1784-425_1784-422delinsCCTG
ENST00000407439.7:c.1793-422_1793-419delinsCCTG	ENSP00000385614.3:n.1793-422_1793-419delinsCCTG
ENST00000535120.1:n.83-425_83-422delinsCCTG
NM_005590.3:c.1783+904_1783+907delinsCCTG	NP_005581.2:n.1783+904_1783+907delinsCCTG
NM_005591.3:c.1784-422_1784-419delinsCCTG , LRG_85t1:c.1784-422_1784-419delinsCCTG	NP_005582.1:n.1784-422_1784-419delinsCCTG
XM_005274008.2:c.1316-422_1316-419delinsCCTG	XP_005274065.1:n.1316-422_1316-419delinsCCTG
XM_006718842.2:c.1784-425_1784-422delinsCCTG	XP_006718905.1:n.1784-425_1784-422delinsCCTG
XM_011542837.1:c.1784-422_1784-419delinsCCTG	XP_011541139.1:n.1784-422_1784-419delinsCCTG
XR_947828.1:n.2080-422_2080-419delinsCCTG
NM_001330347.1:c.1784-425_1784-422delinsCCTG	NP_001317276.1:n.1784-425_1784-422delinsCCTG
XM_005274008.3:c.1316-422_1316-419delinsCCTG	XP_005274065.1:n.1316-422_1316-419delinsCCTG
XM_006718842.3:c.1784-425_1784-422delinsCCTG	XP_006718905.1:n.1784-425_1784-422delinsCCTG
XM_011542837.2:c.1784-422_1784-419delinsCCTG	XP_011541139.1:n.1784-422_1784-419delinsCCTG
XM_017017772.1:c.1784-422_1784-419delinsCCTG	XP_016873261.1:n.1784-422_1784-419delinsCCTG
XR_947828.2:n.2080-422_2080-419delinsCCTG
NM_001330347.2:c.1784-425_1784-422delinsCCTG	NP_001317276.1:n.1784-425_1784-422delinsCCTG
NM_005590.4:c.1783+904_1783+907delinsCCTG	NP_005581.2:n.1783+904_1783+907delinsCCTG
NM_005591.4:c.1784-422_1784-419delinsCCTG MANE Select	NP_005582.1:n.1784-422_1784-419delinsCCTG