Canonical Allele Identifier: CA2574952529

Gene: MRE11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94445818_94445820del , CM000673.2:g.94445818_94445820del	GRCh38
NC_000011.9:g.94178984_94178986del , CM000673.1:g.94178984_94178986del	GRCh37
NC_000011.8:g.93818632_93818634del	NCBI36
NG_007261.1:g.53058_53060del , LRG_85:g.53058_53060del

Transcript Alleles

HGVS	Amino-acid change
ENST00000323929.8:c.1860_1862del MANE Select	ENSP00000325863.4:p.Ile621del
ENST00000323929.7:c.1860_1862del	ENSP00000325863.3:p.Ile621del
ENST00000323977.7:c.1783+1402_1783+1404del	ENSP00000326094.3:n.1783+1402_1783+1404de...
ENST00000393241.8:c.1857_1859del	ENSP00000376933.4:p.Ile620del
ENST00000407439.7:c.1869_1871del	ENSP00000385614.3:p.Ile624del
ENST00000535120.1:n.156_158del
NM_005590.3:c.1783+1402_1783+1404del	NP_005581.2:n.1783+1402_1783+1404del
NM_005591.3:c.1860_1862del , LRG_85t1:c.1860_1862del	NP_005582.1:p.Ile621del
XM_005274008.2:c.1392_1394del	XP_005274065.1:p.Ile465del
XM_006718842.2:c.1857_1859del	XP_006718905.1:p.Ile620del
XM_011542837.1:c.1860_1862del	XP_011541139.1:p.Ile621del
XR_947828.1:n.2156_2158del
NM_001330347.1:c.1857_1859del	NP_001317276.1:p.Ile620del
XM_005274008.3:c.1392_1394del	XP_005274065.1:p.Ile465del
XM_006718842.3:c.1857_1859del	XP_006718905.1:p.Ile620del
XM_011542837.2:c.1860_1862del	XP_011541139.1:p.Ile621del
XM_017017772.1:c.1860_1862del	XP_016873261.1:p.Ile621del
XR_947828.2:n.2156_2158del
NM_001330347.2:c.1857_1859del	NP_001317276.1:p.Ile620del
NM_005590.4:c.1783+1402_1783+1404del	NP_005581.2:n.1783+1402_1783+1404del
NM_005591.4:c.1860_1862del MANE Select	NP_005582.1:p.Ile621del