Canonical Allele Identifier: CA1992441542

Gene: MRE11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94445635_94445636delinsCT , CM000673.2:g.94445635_94445636delinsCT	GRCh38
NC_000011.9:g.94178801_94178802delinsCT , CM000673.1:g.94178801_94178802delinsCT	GRCh37
NC_000011.8:g.93818449_93818450delinsCT	NCBI36
NG_007261.1:g.53239_53240delinsAG , LRG_85:g.53239_53240delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323929.8:c.1867+174_1867+175delinsAG MANE Select	ENSP00000325863.4:n.1867+174_1867+175delinsAG
ENST00000323929.7:c.1867+174_1867+175delinsAG	ENSP00000325863.3:n.1867+174_1867+175delinsAG
ENST00000323977.7:c.1783+1583_1783+1584delinsAG	ENSP00000326094.3:n.1783+1583_1783+1584delinsAG
ENST00000393241.8:c.1864+174_1864+175delinsAG	ENSP00000376933.4:n.1864+174_1864+175delinsAG
ENST00000407439.7:c.1876+174_1876+175delinsAG	ENSP00000385614.3:n.1876+174_1876+175delinsAG
NM_005590.3:c.1783+1583_1783+1584delinsAG	NP_005581.2:n.1783+1583_1783+1584delinsAG
NM_005591.3:c.1867+174_1867+175delinsAG , LRG_85t1:c.1867+174_1867+175delinsAG	NP_005582.1:n.1867+174_1867+175delinsAG
XM_005274008.2:c.1399+174_1399+175delinsAG	XP_005274065.1:n.1399+174_1399+175delinsAG
XM_006718842.2:c.1864+174_1864+175delinsAG	XP_006718905.1:n.1864+174_1864+175delinsAG
XM_011542837.1:c.1867+174_1867+175delinsAG	XP_011541139.1:n.1867+174_1867+175delinsAG
XR_947828.1:n.2163+174_2163+175delinsAG
NM_001330347.1:c.1864+174_1864+175delinsAG	NP_001317276.1:n.1864+174_1864+175delinsAG
XM_005274008.3:c.1399+174_1399+175delinsAG	XP_005274065.1:n.1399+174_1399+175delinsAG
XM_006718842.3:c.1864+174_1864+175delinsAG	XP_006718905.1:n.1864+174_1864+175delinsAG
XM_011542837.2:c.1867+174_1867+175delinsAG	XP_011541139.1:n.1867+174_1867+175delinsAG
XM_017017772.1:c.1867+174_1867+175delinsAG	XP_016873261.1:n.1867+174_1867+175delinsAG
XR_947828.2:n.2163+174_2163+175delinsAG
NM_001330347.2:c.1864+174_1864+175delinsAG	NP_001317276.1:n.1864+174_1864+175delinsAG
NM_005590.4:c.1783+1583_1783+1584delinsAG	NP_005581.2:n.1783+1583_1783+1584delinsAG
NM_005591.4:c.1867+174_1867+175delinsAG MANE Select	NP_005582.1:n.1867+174_1867+175delinsAG