Canonical Allele Identifier: CA382377579
Gene: MRE11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94478820A>C , CM000673.2:g.94478820A>C GRCh38
NC_000011.9:g.94211986A>C , CM000673.1:g.94211986A>C GRCh37
NC_000011.8:g.93851634A>C NCBI36
NG_007261.1:g.20055T>G , LRG_85:g.20055T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000323929.8:c.459T>G MANE Select ENSP00000325863.4:p.Phe153Leu
ENST00000323929.7:c.459T>G ENSP00000325863.3:p.Phe153Leu
ENST00000323977.7:c.459T>G ENSP00000326094.3:p.Phe153Leu
ENST00000393241.8:c.459T>G ENSP00000376933.4:p.Phe153Leu
ENST00000407439.7:c.468T>G ENSP00000385614.3:p.Phe156Leu
ENST00000540013.5:c.459T>G ENSP00000440986.1:p.Phe153Leu
ENST00000541157.5:n.535T>G
NM_005590.3:c.459T>G NP_005581.2:p.Phe153Leu
NM_005591.3:c.459T>G , LRG_85t1:c.459T>G NP_005582.1:p.Phe153Leu
XM_005274008.2:c.-10T>G XP_005274065.1:n.-10T>G
XM_006718842.2:c.459T>G XP_006718905.1:p.Phe153Leu
XM_011542837.1:c.459T>G XP_011541139.1:p.Phe153Leu
XR_947828.1:n.755T>G
NM_001330347.1:c.459T>G NP_001317276.1:p.Phe153Leu
XM_005274008.3:c.-10T>G XP_005274065.1:n.-10T>G
XM_006718842.3:c.459T>G XP_006718905.1:p.Phe153Leu
XM_011542837.2:c.459T>G XP_011541139.1:p.Phe153Leu
XM_017017772.1:c.459T>G XP_016873261.1:p.Phe153Leu
XR_947828.2:n.755T>G
NM_001330347.2:c.459T>G NP_001317276.1:p.Phe153Leu
NM_005590.4:c.459T>G NP_005581.2:p.Phe153Leu
NM_005591.4:c.459T>G MANE Select NP_005582.1:p.Phe153Leu