Canonical Allele Identifier: CA2580085069

Gene: MRE11

Linked Data

• ClinVar Variation Id: 2199339
• ClinVar RCV Id: RCV002624826

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94464093_94464094delinsTG , CM000673.2:g.94464093_94464094delinsTG	GRCh38
NC_000011.9:g.94197259_94197260delinsTG , CM000673.1:g.94197259_94197260delinsTG	GRCh37
NC_000011.8:g.93836907_93836908delinsTG	NCBI36
NG_007261.1:g.34781_34782delinsCA , LRG_85:g.34781_34782delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000323929.8:c.1225+19_1225+20delinsCA MANE Select	ENSP00000325863.4:n.1225+19_1225+20delins...
ENST00000323929.7:c.1225+19_1225+20delinsCA	ENSP00000325863.3:n.1225+19_1225+20delins...
ENST00000323977.7:c.1225+19_1225+20delinsCA	ENSP00000326094.3:n.1225+19_1225+20delins...
ENST00000393241.8:c.1225+19_1225+20delinsCA	ENSP00000376933.4:n.1225+19_1225+20delins...
ENST00000407439.7:c.1234+19_1234+20delinsCA	ENSP00000385614.3:n.1234+19_1234+20delins...
NM_005590.3:c.1225+19_1225+20delinsCA	NP_005581.2:n.1225+19_1225+20delinsCA
NM_005591.3:c.1225+19_1225+20delinsCA , LRG_85t1:c.1225+19_1225+20delinsCA	NP_005582.1:n.1225+19_1225+20delinsCA
XM_005274008.2:c.757+19_757+20delinsCA	XP_005274065.1:n.757+19_757+20delinsCA
XM_006718842.2:c.1225+19_1225+20delinsCA	XP_006718905.1:n.1225+19_1225+20delinsCA
XM_011542837.1:c.1225+19_1225+20delinsCA	XP_011541139.1:n.1225+19_1225+20delinsCA
XR_947828.1:n.1521+19_1521+20delinsCA
NM_001330347.1:c.1225+19_1225+20delinsCA	NP_001317276.1:n.1225+19_1225+20delinsCA
XM_005274008.3:c.757+19_757+20delinsCA	XP_005274065.1:n.757+19_757+20delinsCA
XM_006718842.3:c.1225+19_1225+20delinsCA	XP_006718905.1:n.1225+19_1225+20delinsCA
XM_011542837.2:c.1225+19_1225+20delinsCA	XP_011541139.1:n.1225+19_1225+20delinsCA
XM_017017772.1:c.1225+19_1225+20delinsCA	XP_016873261.1:n.1225+19_1225+20delinsCA
XR_947828.2:n.1521+19_1521+20delinsCA
NM_001330347.2:c.1225+19_1225+20delinsCA	NP_001317276.1:n.1225+19_1225+20delinsCA
NM_005590.4:c.1225+19_1225+20delinsCA	NP_005581.2:n.1225+19_1225+20delinsCA
NM_005591.4:c.1225+19_1225+20delinsCA MANE Select	NP_005582.1:n.1225+19_1225+20delinsCA