Canonical Allele Identifier: CA476280151

Gene: MRE11

Linked Data

• gnomAD v4: 11-94445886-A-C
• MyVariant Identifiers: chr11:g.94179052A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94445886A>C , CM000673.2:g.94445886A>C	GRCh38
NC_000011.9:g.94179052A>C , CM000673.1:g.94179052A>C	GRCh37
NC_000011.8:g.93818700A>C	NCBI36
NG_007261.1:g.52989T>G , LRG_85:g.52989T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323929.8:c.1791T>G MANE Select	ENSP00000325863.4:p.Thr597=
ENST00000323929.7:c.1791T>G	ENSP00000325863.3:p.Thr597=
ENST00000323977.7:c.1783+1333T>G	ENSP00000326094.3:n.1783+1333T>G
ENST00000393241.8:c.1788T>G	ENSP00000376933.4:p.Thr596=
ENST00000407439.7:c.1800T>G	ENSP00000385614.3:p.Thr600=
ENST00000535120.1:n.87T>G
NM_005590.3:c.1783+1333T>G	NP_005581.2:n.1783+1333T>G
NM_005591.3:c.1791T>G , LRG_85t1:c.1791T>G	NP_005582.1:p.Thr597=
XM_005274008.2:c.1323T>G	XP_005274065.1:p.Thr441=
XM_006718842.2:c.1788T>G	XP_006718905.1:p.Thr596=
XM_011542837.1:c.1791T>G	XP_011541139.1:p.Thr597=
XR_947828.1:n.2087T>G
NM_001330347.1:c.1788T>G	NP_001317276.1:p.Thr596=
XM_005274008.3:c.1323T>G	XP_005274065.1:p.Thr441=
XM_006718842.3:c.1788T>G	XP_006718905.1:p.Thr596=
XM_011542837.2:c.1791T>G	XP_011541139.1:p.Thr597=
XM_017017772.1:c.1791T>G	XP_016873261.1:p.Thr597=
XR_947828.2:n.2087T>G
NM_001330347.2:c.1788T>G	NP_001317276.1:p.Thr596=
NM_005590.4:c.1783+1333T>G	NP_005581.2:n.1783+1333T>G
NM_005591.4:c.1791T>G MANE Select	NP_005582.1:p.Thr597=