Canonical Allele Identifier: CA2615588007
Gene: MRE11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94459321_94459324del , CM000673.2:g.94459321_94459324del GRCh38
NC_000011.9:g.94192487_94192490del , CM000673.1:g.94192487_94192490del GRCh37
NC_000011.8:g.93832135_93832138del NCBI36
NG_007261.1:g.39553_39556del , LRG_85:g.39553_39556del

Transcript Alleles

HGVS Amino-acid Change
ENST00000323929.8:c.1500+86_1500+89del MANE Select ENSP00000325863.4:n.1500+86_1500+89del
ENST00000323929.7:c.1500+86_1500+89del ENSP00000325863.3:n.1500+86_1500+89del
ENST00000323977.7:c.1500+86_1500+89del ENSP00000326094.3:n.1500+86_1500+89del
ENST00000393241.8:c.1500+86_1500+89del ENSP00000376933.4:n.1500+86_1500+89del
ENST00000407439.7:c.1509+86_1509+89del ENSP00000385614.3:n.1509+86_1509+89del
NM_005590.3:c.1500+86_1500+89del NP_005581.2:n.1500+86_1500+89del
NM_005591.3:c.1500+86_1500+89del , LRG_85t1:c.1500+86_1500+89del NP_005582.1:n.1500+86_1500+89del
XM_005274008.2:c.1032+86_1032+89del XP_005274065.1:n.1032+86_1032+89del
XM_006718842.2:c.1500+86_1500+89del XP_006718905.1:n.1500+86_1500+89del
XM_011542837.1:c.1500+86_1500+89del XP_011541139.1:n.1500+86_1500+89del
XR_947828.1:n.1796+86_1796+89del
NM_001330347.1:c.1500+86_1500+89del NP_001317276.1:n.1500+86_1500+89del
XM_005274008.3:c.1032+86_1032+89del XP_005274065.1:n.1032+86_1032+89del
XM_006718842.3:c.1500+86_1500+89del XP_006718905.1:n.1500+86_1500+89del
XM_011542837.2:c.1500+86_1500+89del XP_011541139.1:n.1500+86_1500+89del
XM_017017772.1:c.1500+86_1500+89del XP_016873261.1:n.1500+86_1500+89del
XR_947828.2:n.1796+86_1796+89del
NM_001330347.2:c.1500+86_1500+89del NP_001317276.1:n.1500+86_1500+89del
NM_005590.4:c.1500+86_1500+89del NP_005581.2:n.1500+86_1500+89del
NM_005591.4:c.1500+86_1500+89del MANE Select NP_005582.1:n.1500+86_1500+89del