Canonical Allele Identifier: CA382377478
Gene: MRE11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94478797T>A , CM000673.2:g.94478797T>A GRCh38
NC_000011.9:g.94211963T>A , CM000673.1:g.94211963T>A GRCh37
NC_000011.8:g.93851611T>A NCBI36
NG_007261.1:g.20078A>T , LRG_85:g.20078A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000323929.8:c.482A>T MANE Select ENSP00000325863.4:p.Lys161Met
ENST00000323929.7:c.482A>T ENSP00000325863.3:p.Lys161Met
ENST00000323977.7:c.482A>T ENSP00000326094.3:p.Lys161Met
ENST00000393241.8:c.482A>T ENSP00000376933.4:p.Lys161Met
ENST00000407439.7:c.491A>T ENSP00000385614.3:p.Lys164Met
ENST00000540013.5:c.482A>T ENSP00000440986.1:p.Lys161Met
ENST00000541157.5:n.558A>T
NM_005590.3:c.482A>T NP_005581.2:p.Lys161Met
NM_005591.3:c.482A>T , LRG_85t1:c.482A>T NP_005582.1:p.Lys161Met
XM_005274008.2:c.14A>T XP_005274065.1:p.Lys5Met
XM_006718842.2:c.482A>T XP_006718905.1:p.Lys161Met
XM_011542837.1:c.482A>T XP_011541139.1:p.Lys161Met
XR_947828.1:n.778A>T
NM_001330347.1:c.482A>T NP_001317276.1:p.Lys161Met
XM_005274008.3:c.14A>T XP_005274065.1:p.Lys5Met
XM_006718842.3:c.482A>T XP_006718905.1:p.Lys161Met
XM_011542837.2:c.482A>T XP_011541139.1:p.Lys161Met
XM_017017772.1:c.482A>T XP_016873261.1:p.Lys161Met
XR_947828.2:n.778A>T
NM_001330347.2:c.482A>T NP_001317276.1:p.Lys161Met
NM_005590.4:c.482A>T NP_005581.2:p.Lys161Met
NM_005591.4:c.482A>T MANE Select NP_005582.1:p.Lys161Met