Canonical Allele Identifier: CA382373034
Gene: MRE11 HGNC NCBI

Linked Data

ClinVar Variation Id: 822207
ClinVar RCV Id: RCV001017371
dbSNP Id: rs1591681256

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94464223C>T , CM000673.2:g.94464223C>T GRCh38
NC_000011.9:g.94197389C>T , CM000673.1:g.94197389C>T GRCh37
NC_000011.8:g.93837037C>T NCBI36
NG_007261.1:g.34652G>A , LRG_85:g.34652G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000323929.8:c.1115G>A MANE Select ENSP00000325863.4:p.Gly372Asp
ENST00000323929.7:c.1115G>A ENSP00000325863.3:p.Gly372Asp
ENST00000323977.7:c.1115G>A ENSP00000326094.3:p.Gly372Asp
ENST00000393241.8:c.1115G>A ENSP00000376933.4:p.Gly372Asp
ENST00000407439.7:c.1124G>A ENSP00000385614.3:p.Gly375Asp
NM_005590.3:c.1115G>A NP_005581.2:p.Gly372Asp
NM_005591.3:c.1115G>A , LRG_85t1:c.1115G>A NP_005582.1:p.Gly372Asp
XM_005274008.2:c.647G>A XP_005274065.1:p.Gly216Asp
XM_006718842.2:c.1115G>A XP_006718905.1:p.Gly372Asp
XM_011542837.1:c.1115G>A XP_011541139.1:p.Gly372Asp
XR_947828.1:n.1411G>A
NM_001330347.1:c.1115G>A NP_001317276.1:p.Gly372Asp
XM_005274008.3:c.647G>A XP_005274065.1:p.Gly216Asp
XM_006718842.3:c.1115G>A XP_006718905.1:p.Gly372Asp
XM_011542837.2:c.1115G>A XP_011541139.1:p.Gly372Asp
XM_017017772.1:c.1115G>A XP_016873261.1:p.Gly372Asp
XR_947828.2:n.1411G>A
NM_001330347.2:c.1115G>A NP_001317276.1:p.Gly372Asp
NM_005590.4:c.1115G>A NP_005581.2:p.Gly372Asp
NM_005591.4:c.1115G>A MANE Select NP_005582.1:p.Gly372Asp