Canonical Allele Identifier: CA476279802

Gene: MRE11

Linked Data

• MyVariant Identifiers: chr11:g.94178983A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94445817A>T , CM000673.2:g.94445817A>T	GRCh38
NC_000011.9:g.94178983A>T , CM000673.1:g.94178983A>T	GRCh37
NC_000011.8:g.93818631A>T	NCBI36
NG_007261.1:g.53058T>A , LRG_85:g.53058T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000323929.8:c.1860T>A MANE Select	ENSP00000325863.4:p.Ile620=
ENST00000323929.7:c.1860T>A	ENSP00000325863.3:p.Ile620=
ENST00000323977.7:c.1783+1402T>A	ENSP00000326094.3:n.1783+1402T>A
ENST00000393241.8:c.1857T>A	ENSP00000376933.4:p.Ile619=
ENST00000407439.7:c.1869T>A	ENSP00000385614.3:p.Ile623=
ENST00000535120.1:n.156T>A
NM_005590.3:c.1783+1402T>A	NP_005581.2:n.1783+1402T>A
NM_005591.3:c.1860T>A , LRG_85t1:c.1860T>A	NP_005582.1:p.Ile620=
XM_005274008.2:c.1392T>A	XP_005274065.1:p.Ile464=
XM_006718842.2:c.1857T>A	XP_006718905.1:p.Ile619=
XM_011542837.1:c.1860T>A	XP_011541139.1:p.Ile620=
XR_947828.1:n.2156T>A
NM_001330347.1:c.1857T>A	NP_001317276.1:p.Ile619=
XM_005274008.3:c.1392T>A	XP_005274065.1:p.Ile464=
XM_006718842.3:c.1857T>A	XP_006718905.1:p.Ile619=
XM_011542837.2:c.1860T>A	XP_011541139.1:p.Ile620=
XM_017017772.1:c.1860T>A	XP_016873261.1:p.Ile620=
XR_947828.2:n.2156T>A
NM_001330347.2:c.1857T>A	NP_001317276.1:p.Ile619=
NM_005590.4:c.1783+1402T>A	NP_005581.2:n.1783+1402T>A
NM_005591.4:c.1860T>A MANE Select	NP_005582.1:p.Ile620=