Canonical Allele Identifier: CA382374047

Gene: MRE11

Linked Data

• ClinVar Variation Id: 1681551
• ClinVar RCV Id: RCV002239096
• dbSNP Id: rs2134831001
• MyVariant Identifiers: chr11:g.94169013G>T (hg19) ; chr11:g.94435847G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94435847G>T , CM000673.2:g.94435847G>T	GRCh38
NC_000011.9:g.94169013G>T , CM000673.1:g.94169013G>T	GRCh37
NC_000011.8:g.93808661G>T	NCBI36
NG_007261.1:g.63028C>A , LRG_85:g.63028C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000323929.8:c.1979C>A MANE Select	ENSP00000325863.4:p.Ser660Ter
ENST00000323929.7:c.1979C>A	ENSP00000325863.3:p.Ser660Ter
ENST00000323977.7:c.1895C>A	ENSP00000326094.3:p.Ser632Ter
ENST00000393241.8:c.1976C>A	ENSP00000376933.4:p.Ser659Ter
ENST00000407439.7:c.1988C>A	ENSP00000385614.3:p.Ser663Ter
NM_005590.3:c.1895C>A	NP_005581.2:p.Ser632Ter
NM_005591.3:c.1979C>A , LRG_85t1:c.1979C>A	NP_005582.1:p.Ser660Ter
XM_005274008.2:c.1511C>A	XP_005274065.1:p.Ser504Ter
XM_006718842.2:c.1976C>A	XP_006718905.1:p.Ser659Ter
XM_011542837.1:c.1979C>A	XP_011541139.1:p.Ser660Ter
XR_947828.1:n.2275C>A
NM_001330347.1:c.1976C>A	NP_001317276.1:p.Ser659Ter
XM_005274008.3:c.1511C>A	XP_005274065.1:p.Ser504Ter
XM_006718842.3:c.1976C>A	XP_006718905.1:p.Ser659Ter
XM_011542837.2:c.1979C>A	XP_011541139.1:p.Ser660Ter
XM_017017772.1:c.1979C>A	XP_016873261.1:p.Ser660Ter
XR_947828.2:n.2275C>A
NM_001330347.2:c.1976C>A	NP_001317276.1:p.Ser659Ter
NM_005590.4:c.1895C>A	NP_005581.2:p.Ser632Ter
NM_005591.4:c.1979C>A MANE Select	NP_005582.1:p.Ser660Ter