Canonical Allele Identifier: CA382372904
Gene: MRE11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94464187T>G , CM000673.2:g.94464187T>G GRCh38
NC_000011.9:g.94197353T>G , CM000673.1:g.94197353T>G GRCh37
NC_000011.8:g.93837001T>G NCBI36
NG_007261.1:g.34688A>C , LRG_85:g.34688A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000323929.8:c.1151A>C MANE Select ENSP00000325863.4:p.Lys384Thr
ENST00000323929.7:c.1151A>C ENSP00000325863.3:p.Lys384Thr
ENST00000323977.7:c.1151A>C ENSP00000326094.3:p.Lys384Thr
ENST00000393241.8:c.1151A>C ENSP00000376933.4:p.Lys384Thr
ENST00000407439.7:c.1160A>C ENSP00000385614.3:p.Lys387Thr
NM_005590.3:c.1151A>C NP_005581.2:p.Lys384Thr
NM_005591.3:c.1151A>C , LRG_85t1:c.1151A>C NP_005582.1:p.Lys384Thr
XM_005274008.2:c.683A>C XP_005274065.1:p.Lys228Thr
XM_006718842.2:c.1151A>C XP_006718905.1:p.Lys384Thr
XM_011542837.1:c.1151A>C XP_011541139.1:p.Lys384Thr
XR_947828.1:n.1447A>C
NM_001330347.1:c.1151A>C NP_001317276.1:p.Lys384Thr
XM_005274008.3:c.683A>C XP_005274065.1:p.Lys228Thr
XM_006718842.3:c.1151A>C XP_006718905.1:p.Lys384Thr
XM_011542837.2:c.1151A>C XP_011541139.1:p.Lys384Thr
XM_017017772.1:c.1151A>C XP_016873261.1:p.Lys384Thr
XR_947828.2:n.1447A>C
NM_001330347.2:c.1151A>C NP_001317276.1:p.Lys384Thr
NM_005590.4:c.1151A>C NP_005581.2:p.Lys384Thr
NM_005591.4:c.1151A>C MANE Select NP_005582.1:p.Lys384Thr