Canonical Allele Identifier: CA165710
Gene: MRE11 HGNC NCBI

Linked Data

ClinVar Variation Id: 141533
ClinVar RCV Id: RCV000130102 RCV000988623 RCV001376961
dbSNP Id: rs587781822
gnomAD v4: 11-94435901-T-C
MyVariant Identifiers: chr11:g.94169067T>C (hg19) chr11:g.94435901T>C (hg38)
PubMed: PMID:25801821 PMID:26556299
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94435901T>C , CM000673.2:g.94435901T>C GRCh38
NC_000011.9:g.94169067T>C , CM000673.1:g.94169067T>C GRCh37
NC_000011.8:g.93808715T>C NCBI36
NG_007261.1:g.62974A>G , LRG_85:g.62974A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000323929.8:c.1927-2A>G MANE Select ENSP00000325863.4:n.1927-2A>G
ENST00000323929.7:c.1927-2A>G ENSP00000325863.3:n.1927-2A>G
ENST00000323977.7:c.1843-2A>G ENSP00000326094.3:n.1843-2A>G
ENST00000393241.8:c.1924-2A>G ENSP00000376933.4:n.1924-2A>G
ENST00000407439.7:c.1936-2A>G ENSP00000385614.3:n.1936-2A>G
NM_005590.3:c.1843-2A>G NP_005581.2:n.1843-2A>G
NM_005591.3:c.1927-2A>G , LRG_85t1:c.1927-2A>G NP_005582.1:n.1927-2A>G
XM_005274008.2:c.1459-2A>G XP_005274065.1:n.1459-2A>G
XM_006718842.2:c.1924-2A>G XP_006718905.1:n.1924-2A>G
XM_011542837.1:c.1927-2A>G XP_011541139.1:n.1927-2A>G
XR_947828.1:n.2223-2A>G
NM_001330347.1:c.1924-2A>G NP_001317276.1:n.1924-2A>G
XM_005274008.3:c.1459-2A>G XP_005274065.1:n.1459-2A>G
XM_006718842.3:c.1924-2A>G XP_006718905.1:n.1924-2A>G
XM_011542837.2:c.1927-2A>G XP_011541139.1:n.1927-2A>G
XM_017017772.1:c.1927-2A>G XP_016873261.1:n.1927-2A>G
XR_947828.2:n.2223-2A>G
NM_001330347.2:c.1924-2A>G NP_001317276.1:n.1924-2A>G
NM_005590.4:c.1843-2A>G NP_005581.2:n.1843-2A>G
NM_005591.4:c.1927-2A>G MANE Select NP_005582.1:n.1927-2A>G
Search 100 bp 5'
Search 100 bp 3'