Canonical Allele Identifier: CA382366224

Gene: MRE11

Linked Data

• dbSNP Id: rs1945911171
• gnomAD v4: 11-94445814-T-C
• MyVariant Identifiers: chr11:g.94178980T>C (hg19) ; chr11:g.94445814T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94445814T>C , CM000673.2:g.94445814T>C	GRCh38
NC_000011.9:g.94178980T>C , CM000673.1:g.94178980T>C	GRCh37
NC_000011.8:g.93818628T>C	NCBI36
NG_007261.1:g.53061A>G , LRG_85:g.53061A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000323929.8:c.1863A>G MANE Select	ENSP00000325863.4:p.Ile621Met
ENST00000323929.7:c.1863A>G	ENSP00000325863.3:p.Ile621Met
ENST00000323977.7:c.1783+1405A>G	ENSP00000326094.3:n.1783+1405A>G
ENST00000393241.8:c.1860A>G	ENSP00000376933.4:p.Ile620Met
ENST00000407439.7:c.1872A>G	ENSP00000385614.3:p.Ile624Met
ENST00000535120.1:n.159A>G
NM_005590.3:c.1783+1405A>G	NP_005581.2:n.1783+1405A>G
NM_005591.3:c.1863A>G , LRG_85t1:c.1863A>G	NP_005582.1:p.Ile621Met
XM_005274008.2:c.1395A>G	XP_005274065.1:p.Ile465Met
XM_006718842.2:c.1860A>G	XP_006718905.1:p.Ile620Met
XM_011542837.1:c.1863A>G	XP_011541139.1:p.Ile621Met
XR_947828.1:n.2159A>G
NM_001330347.1:c.1860A>G	NP_001317276.1:p.Ile620Met
XM_005274008.3:c.1395A>G	XP_005274065.1:p.Ile465Met
XM_006718842.3:c.1860A>G	XP_006718905.1:p.Ile620Met
XM_011542837.2:c.1863A>G	XP_011541139.1:p.Ile621Met
XM_017017772.1:c.1863A>G	XP_016873261.1:p.Ile621Met
XR_947828.2:n.2159A>G
NM_001330347.2:c.1860A>G	NP_001317276.1:p.Ile620Met
NM_005590.4:c.1783+1405A>G	NP_005581.2:n.1783+1405A>G
NM_005591.4:c.1863A>G MANE Select	NP_005582.1:p.Ile621Met