Canonical Allele Identifier: CA1992461034

Gene: MRE11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94459303_94459305delinsAAC , CM000673.2:g.94459303_94459305delinsAAC	GRCh38
NC_000011.9:g.94192469_94192471delinsAAC , CM000673.1:g.94192469_94192471delinsAAC	GRCh37
NC_000011.8:g.93832117_93832119delinsAAC	NCBI36
NG_007261.1:g.39570_39572delinsGTT , LRG_85:g.39570_39572delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323929.8:c.1500+103_1500+105delinsGTT MANE Select	ENSP00000325863.4:n.1500+103_1500+105delinsGTT
ENST00000323929.7:c.1500+103_1500+105delinsGTT	ENSP00000325863.3:n.1500+103_1500+105delinsGTT
ENST00000323977.7:c.1500+103_1500+105delinsGTT	ENSP00000326094.3:n.1500+103_1500+105delinsGTT
ENST00000393241.8:c.1500+103_1500+105delinsGTT	ENSP00000376933.4:n.1500+103_1500+105delinsGTT
ENST00000407439.7:c.1509+103_1509+105delinsGTT	ENSP00000385614.3:n.1509+103_1509+105delinsGTT
NM_005590.3:c.1500+103_1500+105delinsGTT	NP_005581.2:n.1500+103_1500+105delinsGTT
NM_005591.3:c.1500+103_1500+105delinsGTT , LRG_85t1:c.1500+103_1500+105delinsGTT	NP_005582.1:n.1500+103_1500+105delinsGTT
XM_005274008.2:c.1032+103_1032+105delinsGTT	XP_005274065.1:n.1032+103_1032+105delinsGTT
XM_006718842.2:c.1500+103_1500+105delinsGTT	XP_006718905.1:n.1500+103_1500+105delinsGTT
XM_011542837.1:c.1500+103_1500+105delinsGTT	XP_011541139.1:n.1500+103_1500+105delinsGTT
XR_947828.1:n.1796+103_1796+105delinsGTT
NM_001330347.1:c.1500+103_1500+105delinsGTT	NP_001317276.1:n.1500+103_1500+105delinsGTT
XM_005274008.3:c.1032+103_1032+105delinsGTT	XP_005274065.1:n.1032+103_1032+105delinsGTT
XM_006718842.3:c.1500+103_1500+105delinsGTT	XP_006718905.1:n.1500+103_1500+105delinsGTT
XM_011542837.2:c.1500+103_1500+105delinsGTT	XP_011541139.1:n.1500+103_1500+105delinsGTT
XM_017017772.1:c.1500+103_1500+105delinsGTT	XP_016873261.1:n.1500+103_1500+105delinsGTT
XR_947828.2:n.1796+103_1796+105delinsGTT
NM_001330347.2:c.1500+103_1500+105delinsGTT	NP_001317276.1:n.1500+103_1500+105delinsGTT
NM_005590.4:c.1500+103_1500+105delinsGTT	NP_005581.2:n.1500+103_1500+105delinsGTT
NM_005591.4:c.1500+103_1500+105delinsGTT MANE Select	NP_005582.1:n.1500+103_1500+105delinsGTT