Canonical Allele Identifier: CA382366939

Gene: MRE11

Linked Data

• MyVariant Identifiers: chr11:g.94179058T>A (hg19) ; chr11:g.94445892T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94445892T>A , CM000673.2:g.94445892T>A	GRCh38
NC_000011.9:g.94179058T>A , CM000673.1:g.94179058T>A	GRCh37
NC_000011.8:g.93818706T>A	NCBI36
NG_007261.1:g.52983A>T , LRG_85:g.52983A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323929.8:c.1785A>T MANE Select	ENSP00000325863.4:p.Ala595=
ENST00000323929.7:c.1785A>T	ENSP00000325863.3:p.Ala595=
ENST00000323977.7:c.1783+1327A>T	ENSP00000326094.3:n.1783+1327A>T
ENST00000393241.8:c.1784-2A>T	ENSP00000376933.4:n.1784-2A>T
ENST00000407439.7:c.1794A>T	ENSP00000385614.3:p.Ala598=
ENST00000535120.1:n.83-2A>T
NM_005590.3:c.1783+1327A>T	NP_005581.2:n.1783+1327A>T
NM_005591.3:c.1785A>T , LRG_85t1:c.1785A>T	NP_005582.1:p.Ala595=
XM_005274008.2:c.1317A>T	XP_005274065.1:p.Ala439=
XM_006718842.2:c.1784-2A>T	XP_006718905.1:n.1784-2A>T
XM_011542837.1:c.1785A>T	XP_011541139.1:p.Ala595=
XR_947828.1:n.2081A>T
NM_001330347.1:c.1784-2A>T	NP_001317276.1:n.1784-2A>T
XM_005274008.3:c.1317A>T	XP_005274065.1:p.Ala439=
XM_006718842.3:c.1784-2A>T	XP_006718905.1:n.1784-2A>T
XM_011542837.2:c.1785A>T	XP_011541139.1:p.Ala595=
XM_017017772.1:c.1785A>T	XP_016873261.1:p.Ala595=
XR_947828.2:n.2081A>T
NM_001330347.2:c.1784-2A>T	NP_001317276.1:n.1784-2A>T
NM_005590.4:c.1783+1327A>T	NP_005581.2:n.1783+1327A>T
NM_005591.4:c.1785A>T MANE Select	NP_005582.1:p.Ala595=