Canonical Allele Identifier: CA1992441562

Gene: MRE11

Linked Data

• dbSNP Id: rs1945905462
• gnomAD v3: 11-94445648-C-CTAT
• gnomAD v4: 11-94445648-C-CTAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94445650_94445651insTTA , CM000673.2:g.94445650_94445651insTTA	GRCh38
NC_000011.9:g.94178816_94178817insTTA , CM000673.1:g.94178816_94178817insTTA	GRCh37
NC_000011.8:g.93818464_93818465insTTA	NCBI36
NG_007261.1:g.53226_53227insATA , LRG_85:g.53226_53227insATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323929.8:c.1867+161_1867+162insATA MANE Select	ENSP00000325863.4:n.1867+161_1867+162insATA
ENST00000323929.7:c.1867+161_1867+162insATA	ENSP00000325863.3:n.1867+161_1867+162insATA
ENST00000323977.7:c.1783+1570_1783+1571insATA	ENSP00000326094.3:n.1783+1570_1783+1571insATA
ENST00000393241.8:c.1864+161_1864+162insATA	ENSP00000376933.4:n.1864+161_1864+162insATA
ENST00000407439.7:c.1876+161_1876+162insATA	ENSP00000385614.3:n.1876+161_1876+162insATA
NM_005590.3:c.1783+1570_1783+1571insATA	NP_005581.2:n.1783+1570_1783+1571insATA
NM_005591.3:c.1867+161_1867+162insATA , LRG_85t1:c.1867+161_1867+162insATA	NP_005582.1:n.1867+161_1867+162insATA
XM_005274008.2:c.1399+161_1399+162insATA	XP_005274065.1:n.1399+161_1399+162insATA
XM_006718842.2:c.1864+161_1864+162insATA	XP_006718905.1:n.1864+161_1864+162insATA
XM_011542837.1:c.1867+161_1867+162insATA	XP_011541139.1:n.1867+161_1867+162insATA
XR_947828.1:n.2163+161_2163+162insATA
NM_001330347.1:c.1864+161_1864+162insATA	NP_001317276.1:n.1864+161_1864+162insATA
XM_005274008.3:c.1399+161_1399+162insATA	XP_005274065.1:n.1399+161_1399+162insATA
XM_006718842.3:c.1864+161_1864+162insATA	XP_006718905.1:n.1864+161_1864+162insATA
XM_011542837.2:c.1867+161_1867+162insATA	XP_011541139.1:n.1867+161_1867+162insATA
XM_017017772.1:c.1867+161_1867+162insATA	XP_016873261.1:n.1867+161_1867+162insATA
XR_947828.2:n.2163+161_2163+162insATA
NM_001330347.2:c.1864+161_1864+162insATA	NP_001317276.1:n.1864+161_1864+162insATA
NM_005590.4:c.1783+1570_1783+1571insATA	NP_005581.2:n.1783+1570_1783+1571insATA
NM_005591.4:c.1867+161_1867+162insATA MANE Select	NP_005582.1:n.1867+161_1867+162insATA