Canonical Allele Identifier: CA1992461078

Gene: MRE11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94459359_94459365delinsTAAAGAC , CM000673.2:g.94459359_94459365delinsTAAAGAC	GRCh38
NC_000011.9:g.94192525_94192531delinsTAAAGAC , CM000673.1:g.94192525_94192531delinsTAAAGAC	GRCh37
NC_000011.8:g.93832173_93832179delinsTAAAGAC	NCBI36
NG_007261.1:g.39510_39516delinsGTCTTTA , LRG_85:g.39510_39516delinsGTCTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323929.8:c.1500+43_1500+49delinsGTCTTTA MANE Select	ENSP00000325863.4:n.1500+43_1500+49delinsGTCTTTA
ENST00000323929.7:c.1500+43_1500+49delinsGTCTTTA	ENSP00000325863.3:n.1500+43_1500+49delinsGTCTTTA
ENST00000323977.7:c.1500+43_1500+49delinsGTCTTTA	ENSP00000326094.3:n.1500+43_1500+49delinsGTCTTTA
ENST00000393241.8:c.1500+43_1500+49delinsGTCTTTA	ENSP00000376933.4:n.1500+43_1500+49delinsGTCTTTA
ENST00000407439.7:c.1509+43_1509+49delinsGTCTTTA	ENSP00000385614.3:n.1509+43_1509+49delinsGTCTTTA
NM_005590.3:c.1500+43_1500+49delinsGTCTTTA	NP_005581.2:n.1500+43_1500+49delinsGTCTTTA
NM_005591.3:c.1500+43_1500+49delinsGTCTTTA , LRG_85t1:c.1500+43_1500+49delinsGTCTTTA	NP_005582.1:n.1500+43_1500+49delinsGTCTTTA
XM_005274008.2:c.1032+43_1032+49delinsGTCTTTA	XP_005274065.1:n.1032+43_1032+49delinsGTCTTTA
XM_006718842.2:c.1500+43_1500+49delinsGTCTTTA	XP_006718905.1:n.1500+43_1500+49delinsGTCTTTA
XM_011542837.1:c.1500+43_1500+49delinsGTCTTTA	XP_011541139.1:n.1500+43_1500+49delinsGTCTTTA
XR_947828.1:n.1796+43_1796+49delinsGTCTTTA
NM_001330347.1:c.1500+43_1500+49delinsGTCTTTA	NP_001317276.1:n.1500+43_1500+49delinsGTCTTTA
XM_005274008.3:c.1032+43_1032+49delinsGTCTTTA	XP_005274065.1:n.1032+43_1032+49delinsGTCTTTA
XM_006718842.3:c.1500+43_1500+49delinsGTCTTTA	XP_006718905.1:n.1500+43_1500+49delinsGTCTTTA
XM_011542837.2:c.1500+43_1500+49delinsGTCTTTA	XP_011541139.1:n.1500+43_1500+49delinsGTCTTTA
XM_017017772.1:c.1500+43_1500+49delinsGTCTTTA	XP_016873261.1:n.1500+43_1500+49delinsGTCTTTA
XR_947828.2:n.1796+43_1796+49delinsGTCTTTA
NM_001330347.2:c.1500+43_1500+49delinsGTCTTTA	NP_001317276.1:n.1500+43_1500+49delinsGTCTTTA
NM_005590.4:c.1500+43_1500+49delinsGTCTTTA	NP_005581.2:n.1500+43_1500+49delinsGTCTTTA
NM_005591.4:c.1500+43_1500+49delinsGTCTTTA MANE Select	NP_005582.1:n.1500+43_1500+49delinsGTCTTTA