Canonical Allele Identifier: CA2574952577
Gene: MRE11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94459315_94459316del , CM000673.2:g.94459315_94459316del GRCh38
NC_000011.9:g.94192481_94192482del , CM000673.1:g.94192481_94192482del GRCh37
NC_000011.8:g.93832129_93832130del NCBI36
NG_007261.1:g.39563_39564del , LRG_85:g.39563_39564del

Transcript Alleles

HGVS Amino-acid Change
ENST00000323929.8:c.1500+96_1500+97del MANE Select ENSP00000325863.4:n.1500+96_1500+97del
ENST00000323929.7:c.1500+96_1500+97del ENSP00000325863.3:n.1500+96_1500+97del
ENST00000323977.7:c.1500+96_1500+97del ENSP00000326094.3:n.1500+96_1500+97del
ENST00000393241.8:c.1500+96_1500+97del ENSP00000376933.4:n.1500+96_1500+97del
ENST00000407439.7:c.1509+96_1509+97del ENSP00000385614.3:n.1509+96_1509+97del
NM_005590.3:c.1500+96_1500+97del NP_005581.2:n.1500+96_1500+97del
NM_005591.3:c.1500+96_1500+97del , LRG_85t1:c.1500+96_1500+97del NP_005582.1:n.1500+96_1500+97del
XM_005274008.2:c.1032+96_1032+97del XP_005274065.1:n.1032+96_1032+97del
XM_006718842.2:c.1500+96_1500+97del XP_006718905.1:n.1500+96_1500+97del
XM_011542837.1:c.1500+96_1500+97del XP_011541139.1:n.1500+96_1500+97del
XR_947828.1:n.1796+96_1796+97del
NM_001330347.1:c.1500+96_1500+97del NP_001317276.1:n.1500+96_1500+97del
XM_005274008.3:c.1032+96_1032+97del XP_005274065.1:n.1032+96_1032+97del
XM_006718842.3:c.1500+96_1500+97del XP_006718905.1:n.1500+96_1500+97del
XM_011542837.2:c.1500+96_1500+97del XP_011541139.1:n.1500+96_1500+97del
XM_017017772.1:c.1500+96_1500+97del XP_016873261.1:n.1500+96_1500+97del
XR_947828.2:n.1796+96_1796+97del
NM_001330347.2:c.1500+96_1500+97del NP_001317276.1:n.1500+96_1500+97del
NM_005590.4:c.1500+96_1500+97del NP_005581.2:n.1500+96_1500+97del
NM_005591.4:c.1500+96_1500+97del MANE Select NP_005582.1:n.1500+96_1500+97del