Canonical Allele Identifier: CA1992442754

Gene: MRE11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94446170_94446172delinsGAC , CM000673.2:g.94446170_94446172delinsGAC	GRCh38
NC_000011.9:g.94179336_94179338delinsGAC , CM000673.1:g.94179336_94179338delinsGAC	GRCh37
NC_000011.8:g.93818984_93818986delinsGAC	NCBI36
NG_007261.1:g.52703_52705delinsGTC , LRG_85:g.52703_52705delinsGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323929.8:c.1784-279_1784-277delinsGTC MANE Select	ENSP00000325863.4:n.1784-279_1784-277delinsGTC
ENST00000323929.7:c.1784-279_1784-277delinsGTC	ENSP00000325863.3:n.1784-279_1784-277delinsGTC
ENST00000323977.7:c.1783+1047_1783+1049delinsGTC	ENSP00000326094.3:n.1783+1047_1783+1049delinsGTC
ENST00000393241.8:c.1784-282_1784-280delinsGTC	ENSP00000376933.4:n.1784-282_1784-280delinsGTC
ENST00000407439.7:c.1793-279_1793-277delinsGTC	ENSP00000385614.3:n.1793-279_1793-277delinsGTC
ENST00000535120.1:n.83-282_83-280delinsGTC
NM_005590.3:c.1783+1047_1783+1049delinsGTC	NP_005581.2:n.1783+1047_1783+1049delinsGTC
NM_005591.3:c.1784-279_1784-277delinsGTC , LRG_85t1:c.1784-279_1784-277delinsGTC	NP_005582.1:n.1784-279_1784-277delinsGTC
XM_005274008.2:c.1316-279_1316-277delinsGTC	XP_005274065.1:n.1316-279_1316-277delinsGTC
XM_006718842.2:c.1784-282_1784-280delinsGTC	XP_006718905.1:n.1784-282_1784-280delinsGTC
XM_011542837.1:c.1784-279_1784-277delinsGTC	XP_011541139.1:n.1784-279_1784-277delinsGTC
XR_947828.1:n.2080-279_2080-277delinsGTC
NM_001330347.1:c.1784-282_1784-280delinsGTC	NP_001317276.1:n.1784-282_1784-280delinsGTC
XM_005274008.3:c.1316-279_1316-277delinsGTC	XP_005274065.1:n.1316-279_1316-277delinsGTC
XM_006718842.3:c.1784-282_1784-280delinsGTC	XP_006718905.1:n.1784-282_1784-280delinsGTC
XM_011542837.2:c.1784-279_1784-277delinsGTC	XP_011541139.1:n.1784-279_1784-277delinsGTC
XM_017017772.1:c.1784-279_1784-277delinsGTC	XP_016873261.1:n.1784-279_1784-277delinsGTC
XR_947828.2:n.2080-279_2080-277delinsGTC
NM_001330347.2:c.1784-282_1784-280delinsGTC	NP_001317276.1:n.1784-282_1784-280delinsGTC
NM_005590.4:c.1783+1047_1783+1049delinsGTC	NP_005581.2:n.1783+1047_1783+1049delinsGTC
NM_005591.4:c.1784-279_1784-277delinsGTC MANE Select	NP_005582.1:n.1784-279_1784-277delinsGTC