Canonical Allele Identifier: CA941030445

Gene: MRE11

Linked Data

• gnomAD v3: 11-94464094-A-AAAAATAACTAGCTTACCTGTTTTTTATTTTTTTACCTCG
• gnomAD v4: 11-94464094-A-AAAAATAACTAGCTTACCTGTTTTTTATTTTTTTACCTCG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94464094_94464095insAAAATAACTAGCTTACCTGTTTTTTATTTTTTTACCTCG , CM000673.2:g.94464094_94464095insAAAATAACTAGCTTACCTGTTTTTTATTTTTTTACCTCG	GRCh38
NC_000011.9:g.94197260_94197261insAAAATAACTAGCTTACCTGTTTTTTATTTTTTTACCTCG , CM000673.1:g.94197260_94197261insAAAATAACTAGCTTACCTGTTTTTTATTTTTTTACCTCG	GRCh37
NC_000011.8:g.93836908_93836909insAAAATAACTAGCTTACCTGTTTTTTATTTTTTTACCTCG	NCBI36
NG_007261.1:g.34780_34781insCGAGGTAAAAAAATAAAAAACAGGTAAGCTAGTTATTTT , LRG_85:g.34780_34781insCGAGGTAAAAAAATAAAAAACAGGTAAGCTAGTTATTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000323929.8:c.1225+18_1225+19insCGAGGTAAAAAAATAAAAAACAGGTAAGCTAGTTATTTT MANE Select	ENSP00000325863.4:n.1225+18_1225+19insCGA...
ENST00000323929.7:c.1225+18_1225+19insCGAGGTAAAAAAATAAAAAACAGGTAAGCTAGTTATTTT	ENSP00000325863.3:n.1225+18_1225+19insCGA...
ENST00000323977.7:c.1225+18_1225+19insCGAGGTAAAAAAATAAAAAACAGGTAAGCTAGTTATTTT	ENSP00000326094.3:n.1225+18_1225+19insCGA...
ENST00000393241.8:c.1225+18_1225+19insCGAGGTAAAAAAATAAAAAACAGGTAAGCTAGTTATTTT	ENSP00000376933.4:n.1225+18_1225+19insCGA...
ENST00000407439.7:c.1234+18_1234+19insCGAGGTAAAAAAATAAAAAACAGGTAAGCTAGTTATTTT	ENSP00000385614.3:n.1234+18_1234+19insCGA...
NM_005590.3:c.1225+18_1225+19insCGAGGTAAAAAAATAAAAAACAGGTAAGCTAGTTATTTT	NP_005581.2:n.1225+18_1225+19insCGAGGTAAA...
NM_005591.3:c.1225+18_1225+19insCGAGGTAAAAAAATAAAAAACAGGTAAGCTAGTTATTTT , LRG_85t1:c.1225+18_1225+19insCGAGGTAAAAAAATAAAAAACAGGTAAGCTAGTTATTTT	NP_005582.1:n.1225+18_1225+19insCGAGGTAAA...
XM_005274008.2:c.757+18_757+19insCGAGGTAAAAAAATAAAAAACAGGTAAGCTAGTTATTTT	XP_005274065.1:n.757+18_757+19insCGAGGTAA...
XM_006718842.2:c.1225+18_1225+19insCGAGGTAAAAAAATAAAAAACAGGTAAGCTAGTTATTTT	XP_006718905.1:n.1225+18_1225+19insCGAGGT...
XM_011542837.1:c.1225+18_1225+19insCGAGGTAAAAAAATAAAAAACAGGTAAGCTAGTTATTTT	XP_011541139.1:n.1225+18_1225+19insCGAGGT...
XR_947828.1:n.1521+18_1521+19insCGAGGTAAAAAAATAAAAAACAGGTAAGCTAGTTATTTT
NM_001330347.1:c.1225+18_1225+19insCGAGGTAAAAAAATAAAAAACAGGTAAGCTAGTTATTTT	NP_001317276.1:n.1225+18_1225+19insCGAGGT...
XM_005274008.3:c.757+18_757+19insCGAGGTAAAAAAATAAAAAACAGGTAAGCTAGTTATTTT	XP_005274065.1:n.757+18_757+19insCGAGGTAA...
XM_006718842.3:c.1225+18_1225+19insCGAGGTAAAAAAATAAAAAACAGGTAAGCTAGTTATTTT	XP_006718905.1:n.1225+18_1225+19insCGAGGT...
XM_011542837.2:c.1225+18_1225+19insCGAGGTAAAAAAATAAAAAACAGGTAAGCTAGTTATTTT	XP_011541139.1:n.1225+18_1225+19insCGAGGT...
XM_017017772.1:c.1225+18_1225+19insCGAGGTAAAAAAATAAAAAACAGGTAAGCTAGTTATTTT	XP_016873261.1:n.1225+18_1225+19insCGAGGT...
XR_947828.2:n.1521+18_1521+19insCGAGGTAAAAAAATAAAAAACAGGTAAGCTAGTTATTTT
NM_001330347.2:c.1225+18_1225+19insCGAGGTAAAAAAATAAAAAACAGGTAAGCTAGTTATTTT	NP_001317276.1:n.1225+18_1225+19insCGAGGT...
NM_005590.4:c.1225+18_1225+19insCGAGGTAAAAAAATAAAAAACAGGTAAGCTAGTTATTTT	NP_005581.2:n.1225+18_1225+19insCGAGGTAAA...
NM_005591.4:c.1225+18_1225+19insCGAGGTAAAAAAATAAAAAACAGGTAAGCTAGTTATTTT MANE Select	NP_005582.1:n.1225+18_1225+19insCGAGGTAAA...