Canonical Allele Identifier: CA1992468969

Gene: MRE11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94464206_94464238delinsCACTGAAAGGTTCAAAACCTCCACTATAGTCCA , CM000673.2:g.94464206_94464238delinsCACTGAAAGGTTCAAAACCTCCACTATAGTCCA	GRCh38
NC_000011.9:g.94197372_94197404delinsCACTGAAAGGTTCAAAACCTCCACTATAGTCCA , CM000673.1:g.94197372_94197404delinsCACTGAAAGGTTCAAAACCTCCACTATAGTCCA	GRCh37
NC_000011.8:g.93837020_93837052delinsCACTGAAAGGTTCAAAACCTCCACTATAGTCCA	NCBI36
NG_007261.1:g.34637_34669delinsTGGACTATAGTGGAGGTTTTGAACCTTTCAGTG , LRG_85:g.34637_34669delinsTGGACTATAGTGGAGGTTTTGAACCTTTCAGTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000323929.8:c.1100_1132delinsTGGACTATAGTGGAGGTTTTGAACCTTTCAGTG MANE Select	ENSP00000325863.4:p.Val367=
ENST00000323929.7:c.1100_1132delinsTGGACTATAGTGGAGGTTTTGAACCTTTCAGTG	ENSP00000325863.3:p.Val367=
ENST00000323977.7:c.1100_1132delinsTGGACTATAGTGGAGGTTTTGAACCTTTCAGTG	ENSP00000326094.3:p.Val367=
ENST00000393241.8:c.1100_1132delinsTGGACTATAGTGGAGGTTTTGAACCTTTCAGTG	ENSP00000376933.4:p.Val367=
ENST00000407439.7:c.1109_1141delinsTGGACTATAGTGGAGGTTTTGAACCTTTCAGTG	ENSP00000385614.3:p.Val370=
NM_005590.3:c.1100_1132delinsTGGACTATAGTGGAGGTTTTGAACCTTTCAGTG	NP_005581.2:p.Val367=
NM_005591.3:c.1100_1132delinsTGGACTATAGTGGAGGTTTTGAACCTTTCAGTG , LRG_85t1:c.1100_1132delinsTGGACTATAGTGGAGGTTTTGAACCTTTCAGTG	NP_005582.1:p.Val367=
XM_005274008.2:c.632_664delinsTGGACTATAGTGGAGGTTTTGAACCTTTCAGTG	XP_005274065.1:p.Val211=
XM_006718842.2:c.1100_1132delinsTGGACTATAGTGGAGGTTTTGAACCTTTCAGTG	XP_006718905.1:p.Val367=
XM_011542837.1:c.1100_1132delinsTGGACTATAGTGGAGGTTTTGAACCTTTCAGTG	XP_011541139.1:p.Val367=
XR_947828.1:n.1396_1428delinsTGGACTATAGTGGAGGTTTTGAACCTTTCAGTG
NM_001330347.1:c.1100_1132delinsTGGACTATAGTGGAGGTTTTGAACCTTTCAGTG	NP_001317276.1:p.Val367=
XM_005274008.3:c.632_664delinsTGGACTATAGTGGAGGTTTTGAACCTTTCAGTG	XP_005274065.1:p.Val211=
XM_006718842.3:c.1100_1132delinsTGGACTATAGTGGAGGTTTTGAACCTTTCAGTG	XP_006718905.1:p.Val367=
XM_011542837.2:c.1100_1132delinsTGGACTATAGTGGAGGTTTTGAACCTTTCAGTG	XP_011541139.1:p.Val367=
XM_017017772.1:c.1100_1132delinsTGGACTATAGTGGAGGTTTTGAACCTTTCAGTG	XP_016873261.1:p.Val367=
XR_947828.2:n.1396_1428delinsTGGACTATAGTGGAGGTTTTGAACCTTTCAGTG
NM_001330347.2:c.1100_1132delinsTGGACTATAGTGGAGGTTTTGAACCTTTCAGTG	NP_001317276.1:p.Val367=
NM_005590.4:c.1100_1132delinsTGGACTATAGTGGAGGTTTTGAACCTTTCAGTG	NP_005581.2:p.Val367=
NM_005591.4:c.1100_1132delinsTGGACTATAGTGGAGGTTTTGAACCTTTCAGTG MANE Select	NP_005582.1:p.Val367=