Canonical Allele Identifier: CA1992469499

Gene: MRE11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94464410_94464413delinsCTAA , CM000673.2:g.94464410_94464413delinsCTAA	GRCh38
NC_000011.9:g.94197576_94197579delinsCTAA , CM000673.1:g.94197576_94197579delinsCTAA	GRCh37
NC_000011.8:g.93837224_93837227delinsCTAA	NCBI36
NG_007261.1:g.34462_34465delinsTTAG , LRG_85:g.34462_34465delinsTTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323929.8:c.1099-174_1099-171delinsTTAG MANE Select	ENSP00000325863.4:n.1099-174_1099-171delinsTTAG
ENST00000323929.7:c.1099-174_1099-171delinsTTAG	ENSP00000325863.3:n.1099-174_1099-171delinsTTAG
ENST00000323977.7:c.1099-174_1099-171delinsTTAG	ENSP00000326094.3:n.1099-174_1099-171delinsTTAG
ENST00000393241.8:c.1099-174_1099-171delinsTTAG	ENSP00000376933.4:n.1099-174_1099-171delinsTTAG
ENST00000407439.7:c.1108-174_1108-171delinsTTAG	ENSP00000385614.3:n.1108-174_1108-171delinsTTAG
NM_005590.3:c.1099-174_1099-171delinsTTAG	NP_005581.2:n.1099-174_1099-171delinsTTAG
NM_005591.3:c.1099-174_1099-171delinsTTAG , LRG_85t1:c.1099-174_1099-171delinsTTAG	NP_005582.1:n.1099-174_1099-171delinsTTAG
XM_005274008.2:c.631-174_631-171delinsTTAG	XP_005274065.1:n.631-174_631-171delinsTTAG
XM_006718842.2:c.1099-174_1099-171delinsTTAG	XP_006718905.1:n.1099-174_1099-171delinsTTAG
XM_011542837.1:c.1099-174_1099-171delinsTTAG	XP_011541139.1:n.1099-174_1099-171delinsTTAG
XR_947828.1:n.1395-174_1395-171delinsTTAG
NM_001330347.1:c.1099-174_1099-171delinsTTAG	NP_001317276.1:n.1099-174_1099-171delinsTTAG
XM_005274008.3:c.631-174_631-171delinsTTAG	XP_005274065.1:n.631-174_631-171delinsTTAG
XM_006718842.3:c.1099-174_1099-171delinsTTAG	XP_006718905.1:n.1099-174_1099-171delinsTTAG
XM_011542837.2:c.1099-174_1099-171delinsTTAG	XP_011541139.1:n.1099-174_1099-171delinsTTAG
XM_017017772.1:c.1099-174_1099-171delinsTTAG	XP_016873261.1:n.1099-174_1099-171delinsTTAG
XR_947828.2:n.1395-174_1395-171delinsTTAG
NM_001330347.2:c.1099-174_1099-171delinsTTAG	NP_001317276.1:n.1099-174_1099-171delinsTTAG
NM_005590.4:c.1099-174_1099-171delinsTTAG	NP_005581.2:n.1099-174_1099-171delinsTTAG
NM_005591.4:c.1099-174_1099-171delinsTTAG MANE Select	NP_005582.1:n.1099-174_1099-171delinsTTAG