Canonical Allele Identifier: CA1992436600

Gene: MRE11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94478767_94478775delinsTTTTGAAGC , CM000673.2:g.94478767_94478775delinsTTTTGAAGC	GRCh38
NC_000011.9:g.94211933_94211941delinsTTTTGAAGC , CM000673.1:g.94211933_94211941delinsTTTTGAAGC	GRCh37
NC_000011.8:g.93851581_93851589delinsTTTTGAAGC	NCBI36
NG_007261.1:g.20100_20108delinsGCTTCAAAA , LRG_85:g.20100_20108delinsGCTTCAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323929.8:c.504_512delinsGCTTCAAAA MANE Select	ENSP00000325863.4:p.Leu168=
ENST00000323929.7:c.504_512delinsGCTTCAAAA	ENSP00000325863.3:p.Leu168=
ENST00000323977.7:c.504_512delinsGCTTCAAAA	ENSP00000326094.3:p.Leu168=
ENST00000393241.8:c.504_512delinsGCTTCAAAA	ENSP00000376933.4:p.Leu168=
ENST00000407439.7:c.513_521delinsGCTTCAAAA	ENSP00000385614.3:p.Leu171=
ENST00000540013.5:c.504_512delinsGCTTCAAAA	ENSP00000440986.1:p.Leu168=
ENST00000541157.5:n.580_588delinsGCTTCAAAA
NM_005590.3:c.504_512delinsGCTTCAAAA	NP_005581.2:p.Leu168=
NM_005591.3:c.504_512delinsGCTTCAAAA , LRG_85t1:c.504_512delinsGCTTCAAAA	NP_005582.1:p.Leu168=
XM_005274008.2:c.36_44delinsGCTTCAAAA	XP_005274065.1:p.Leu12=
XM_006718842.2:c.504_512delinsGCTTCAAAA	XP_006718905.1:p.Leu168=
XM_011542837.1:c.504_512delinsGCTTCAAAA	XP_011541139.1:p.Leu168=
XR_947828.1:n.800_808delinsGCTTCAAAA
NM_001330347.1:c.504_512delinsGCTTCAAAA	NP_001317276.1:p.Leu168=
XM_005274008.3:c.36_44delinsGCTTCAAAA	XP_005274065.1:p.Leu12=
XM_006718842.3:c.504_512delinsGCTTCAAAA	XP_006718905.1:p.Leu168=
XM_011542837.2:c.504_512delinsGCTTCAAAA	XP_011541139.1:p.Leu168=
XM_017017772.1:c.504_512delinsGCTTCAAAA	XP_016873261.1:p.Leu168=
XR_947828.2:n.800_808delinsGCTTCAAAA
NM_001330347.2:c.504_512delinsGCTTCAAAA	NP_001317276.1:p.Leu168=
NM_005590.4:c.504_512delinsGCTTCAAAA	NP_005581.2:p.Leu168=
NM_005591.4:c.504_512delinsGCTTCAAAA MANE Select	NP_005582.1:p.Leu168=