Canonical Allele Identifier: CA1992468191
Gene: MRE11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94463990_94463994delinsATTTG , CM000673.2:g.94463990_94463994delinsATTTG GRCh38
NC_000011.9:g.94197156_94197160delinsATTTG , CM000673.1:g.94197156_94197160delinsATTTG GRCh37
NC_000011.8:g.93836804_93836808delinsATTTG NCBI36
NG_007261.1:g.34881_34885delinsCAAAT , LRG_85:g.34881_34885delinsCAAAT

Transcript Alleles

HGVS Amino-acid change
ENST00000323929.8:c.1225+119_1225+123delinsCAAAT MANE Select ENSP00000325863.4:n.1225+119_1225+123deli...
ENST00000323929.7:c.1225+119_1225+123delinsCAAAT ENSP00000325863.3:n.1225+119_1225+123deli...
ENST00000323977.7:c.1225+119_1225+123delinsCAAAT ENSP00000326094.3:n.1225+119_1225+123deli...
ENST00000393241.8:c.1225+119_1225+123delinsCAAAT ENSP00000376933.4:n.1225+119_1225+123deli...
ENST00000407439.7:c.1234+119_1234+123delinsCAAAT ENSP00000385614.3:n.1234+119_1234+123deli...
NM_005590.3:c.1225+119_1225+123delinsCAAAT NP_005581.2:n.1225+119_1225+123delinsCAAA...
NM_005591.3:c.1225+119_1225+123delinsCAAAT , LRG_85t1:c.1225+119_1225+123delinsCAAAT NP_005582.1:n.1225+119_1225+123delinsCAAA...
XM_005274008.2:c.757+119_757+123delinsCAAAT XP_005274065.1:n.757+119_757+123delinsCAA...
XM_006718842.2:c.1225+119_1225+123delinsCAAAT XP_006718905.1:n.1225+119_1225+123delinsC...
XM_011542837.1:c.1225+119_1225+123delinsCAAAT XP_011541139.1:n.1225+119_1225+123delinsC...
XR_947828.1:n.1521+119_1521+123delinsCAAAT
NM_001330347.1:c.1225+119_1225+123delinsCAAAT NP_001317276.1:n.1225+119_1225+123delinsC...
XM_005274008.3:c.757+119_757+123delinsCAAAT XP_005274065.1:n.757+119_757+123delinsCAA...
XM_006718842.3:c.1225+119_1225+123delinsCAAAT XP_006718905.1:n.1225+119_1225+123delinsC...
XM_011542837.2:c.1225+119_1225+123delinsCAAAT XP_011541139.1:n.1225+119_1225+123delinsC...
XM_017017772.1:c.1225+119_1225+123delinsCAAAT XP_016873261.1:n.1225+119_1225+123delinsC...
XR_947828.2:n.1521+119_1521+123delinsCAAAT
NM_001330347.2:c.1225+119_1225+123delinsCAAAT NP_001317276.1:n.1225+119_1225+123delinsC...
NM_005590.4:c.1225+119_1225+123delinsCAAAT NP_005581.2:n.1225+119_1225+123delinsCAAA...
NM_005591.4:c.1225+119_1225+123delinsCAAAT MANE Select NP_005582.1:n.1225+119_1225+123delinsCAAA...