Canonical Allele Identifier: CA682020874

Gene: MRE11

Linked Data

• dbSNP Id: rs1465250609
• gnomAD v4: 11-94445684-TC-T
• MyVariant Identifiers: chr11:g.94178851del (hg19) ; chr11:g.94445685del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94445686del , CM000673.2:g.94445686del	GRCh38
NC_000011.9:g.94178852del , CM000673.1:g.94178852del	GRCh37
NC_000011.8:g.93818500del	NCBI36
NG_007261.1:g.53190del , LRG_85:g.53190del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323929.8:c.1867+125del MANE Select	ENSP00000325863.4:n.1867+125del
ENST00000323929.7:c.1867+125del	ENSP00000325863.3:n.1867+125del
ENST00000323977.7:c.1783+1534del	ENSP00000326094.3:n.1783+1534del
ENST00000393241.8:c.1864+125del	ENSP00000376933.4:n.1864+125del
ENST00000407439.7:c.1876+125del	ENSP00000385614.3:n.1876+125del
NM_005590.3:c.1783+1534del	NP_005581.2:n.1783+1534del
NM_005591.3:c.1867+125del , LRG_85t1:c.1867+125del	NP_005582.1:n.1867+125del
XM_005274008.2:c.1399+125del	XP_005274065.1:n.1399+125del
XM_006718842.2:c.1864+125del	XP_006718905.1:n.1864+125del
XM_011542837.1:c.1867+125del	XP_011541139.1:n.1867+125del
XR_947828.1:n.2163+125del
NM_001330347.1:c.1864+125del	NP_001317276.1:n.1864+125del
XM_005274008.3:c.1399+125del	XP_005274065.1:n.1399+125del
XM_006718842.3:c.1864+125del	XP_006718905.1:n.1864+125del
XM_011542837.2:c.1867+125del	XP_011541139.1:n.1867+125del
XM_017017772.1:c.1867+125del	XP_016873261.1:n.1867+125del
XR_947828.2:n.2163+125del
NM_001330347.2:c.1864+125del	NP_001317276.1:n.1864+125del
NM_005590.4:c.1783+1534del	NP_005581.2:n.1783+1534del
NM_005591.4:c.1867+125del MANE Select	NP_005582.1:n.1867+125del