Canonical Allele Identifier: CA1992427014

Gene: MRE11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94471596_94471601delinsAAAGAG , CM000673.2:g.94471596_94471601delinsAAAGAG	GRCh38
NC_000011.9:g.94204762_94204767delinsAAAGAG , CM000673.1:g.94204762_94204767delinsAAAGAG	GRCh37
NC_000011.8:g.93844410_93844415delinsAAAGAG	NCBI36
NG_007261.1:g.27274_27279delinsCTCTTT , LRG_85:g.27274_27279delinsCTCTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000323929.8:c.818_823delinsCTCTTT MANE Select	ENSP00000325863.4:p.Ser273=
ENST00000323929.7:c.818_823delinsCTCTTT	ENSP00000325863.3:p.Ser273=
ENST00000323977.7:c.818_823delinsCTCTTT	ENSP00000326094.3:p.Ser273=
ENST00000393241.8:c.818_823delinsCTCTTT	ENSP00000376933.4:p.Ser273=
ENST00000407439.7:c.827_832delinsCTCTTT	ENSP00000385614.3:p.Ser276=
NM_005590.3:c.818_823delinsCTCTTT	NP_005581.2:p.Ser273=
NM_005591.3:c.818_823delinsCTCTTT , LRG_85t1:c.818_823delinsCTCTTT	NP_005582.1:p.Ser273=
XM_005274008.2:c.350_355delinsCTCTTT	XP_005274065.1:p.Ser117=
XM_006718842.2:c.818_823delinsCTCTTT	XP_006718905.1:p.Ser273=
XM_011542837.1:c.818_823delinsCTCTTT	XP_011541139.1:p.Ser273=
XR_947828.1:n.1114_1119delinsCTCTTT
NM_001330347.1:c.818_823delinsCTCTTT	NP_001317276.1:p.Ser273=
XM_005274008.3:c.350_355delinsCTCTTT	XP_005274065.1:p.Ser117=
XM_006718842.3:c.818_823delinsCTCTTT	XP_006718905.1:p.Ser273=
XM_011542837.2:c.818_823delinsCTCTTT	XP_011541139.1:p.Ser273=
XM_017017772.1:c.818_823delinsCTCTTT	XP_016873261.1:p.Ser273=
XR_947828.2:n.1114_1119delinsCTCTTT
NM_001330347.2:c.818_823delinsCTCTTT	NP_001317276.1:p.Ser273=
NM_005590.4:c.818_823delinsCTCTTT	NP_005581.2:p.Ser273=
NM_005591.4:c.818_823delinsCTCTTT MANE Select	NP_005582.1:p.Ser273=