Canonical Allele Identifier: CA645592520

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9079675_9079676del , CM000674.2:g.9079675_9079676del GRCh38
NC_000012.11:g.9232271_9232272del , CM000674.1:g.9232271_9232272del GRCh37
NC_000012.10:g.9123538_9123539del NCBI36
NG_011717.1:g.41290_41291del
NG_011717.2:g.41290_41291del

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.12:c.2997_2998del (A2M) MANE Select ENSP00000323929.8:p.Glu999AspfsTer23
ENST00000318602.11:c.2997_2998del (A2M) ENSP00000323929.7:p.Glu999AspfsTer23
ENST00000542567.1:n.352_353del (A2M)
ENST00000543436.2:n.451+10239_451+10240del (A2M)
ENST00000545828.1:n.349-6952_349-6951del (A2M)
NM_000014.4:c.2997_2998del (A2M) NP_000005.2:p.Glu999AspfsTer23
XM_006719056.2:c.2997_2998del (A2M) XP_006719119.1:p.Glu999AspfsTer23
NM_000014.5:c.2997_2998del (A2M) NP_000005.2:p.Glu999AspfsTer23
NM_001347423.1:c.2997_2998del (A2M) NP_001334352.1:p.Glu999AspfsTer23
NM_001347424.1:c.2697_2698del (A2M) NP_001334353.1:p.Glu899AspfsTer23
NM_001347425.1:c.2547_2548del (A2M) NP_001334354.1:p.Glu849AspfsTer23
XM_006719056.3:c.2997_2998del (A2M) XP_006719119.1:p.Glu999AspfsTer23
XM_017018683.1:c.*33+21509_*33+21510del (KLRG1) XP_016874172.1:n.*33+21509_*33+21510del
XM_017018684.1:c.*33+21509_*33+21510del (KLRG1) XP_016874173.1:n.*33+21509_*33+21510del
XM_017018685.1:c.*33+21509_*33+21510del (KLRG1) XP_016874174.1:n.*33+21509_*33+21510del
NM_000014.6:c.2997_2998del (A2M) MANE Select NP_000005.3:p.Glu999AspfsTer23
NM_001347423.2:c.2997_2998del (A2M) NP_001334352.2:p.Glu999AspfsTer23
NM_001347424.2:c.2697_2698del (A2M) NP_001334353.2:p.Glu899AspfsTer23
NM_001347425.2:c.2547_2548del (A2M) NP_001334354.2:p.Glu849AspfsTer23