Canonical Allele Identifier: CA1992461252

Gene: MRE11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94459422_94459423delinsTG , CM000673.2:g.94459422_94459423delinsTG	GRCh38
NC_000011.9:g.94192588_94192589delinsTG , CM000673.1:g.94192588_94192589delinsTG	GRCh37
NC_000011.8:g.93832236_93832237delinsTG	NCBI36
NG_007261.1:g.39452_39453delinsCA , LRG_85:g.39452_39453delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323929.8:c.1485_1486delinsCA MANE Select	ENSP00000325863.4:p.Asp495=
ENST00000323929.7:c.1485_1486delinsCA	ENSP00000325863.3:p.Asp495=
ENST00000323977.7:c.1485_1486delinsCA	ENSP00000326094.3:p.Asp495=
ENST00000393241.8:c.1485_1486delinsCA	ENSP00000376933.4:p.Asp495=
ENST00000407439.7:c.1494_1495delinsCA	ENSP00000385614.3:p.Asp498=
NM_005590.3:c.1485_1486delinsCA	NP_005581.2:p.Asp495=
NM_005591.3:c.1485_1486delinsCA , LRG_85t1:c.1485_1486delinsCA	NP_005582.1:p.Asp495=
XM_005274008.2:c.1017_1018delinsCA	XP_005274065.1:p.Asp339=
XM_006718842.2:c.1485_1486delinsCA	XP_006718905.1:p.Asp495=
XM_011542837.1:c.1485_1486delinsCA	XP_011541139.1:p.Asp495=
XR_947828.1:n.1781_1782delinsCA
NM_001330347.1:c.1485_1486delinsCA	NP_001317276.1:p.Asp495=
XM_005274008.3:c.1017_1018delinsCA	XP_005274065.1:p.Asp339=
XM_006718842.3:c.1485_1486delinsCA	XP_006718905.1:p.Asp495=
XM_011542837.2:c.1485_1486delinsCA	XP_011541139.1:p.Asp495=
XM_017017772.1:c.1485_1486delinsCA	XP_016873261.1:p.Asp495=
XR_947828.2:n.1781_1782delinsCA
NM_001330347.2:c.1485_1486delinsCA	NP_001317276.1:p.Asp495=
NM_005590.4:c.1485_1486delinsCA	NP_005581.2:p.Asp495=
NM_005591.4:c.1485_1486delinsCA MANE Select	NP_005582.1:p.Asp495=