Canonical Allele Identifier: CA944576163

Linked Data

dbSNP Id: rs1939081648

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9115873_9115875del , CM000674.2:g.9115873_9115875del GRCh38
NC_000012.11:g.9268469_9268471del , CM000674.1:g.9268469_9268471del GRCh37
NC_000012.10:g.9159736_9159738del NCBI36
NG_011717.1:g.5092_5094del
NG_011717.2:g.5092_5094del

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.12:c.-22_-20del (A2M) MANE Select ENSP00000323929.8:n.-22_-20del
ENST00000318602.11:c.-22_-20del (A2M) ENSP00000323929.7:n.-22_-20del
ENST00000404455.2:c.-17-5_-17-3del (A2M) ENSP00000385710.2:n.-17-5_-17-3del
ENST00000467091.1:n.191_193del (A2M)
ENST00000497324.1:n.147_149del (A2M)
NM_000014.4:c.-22_-20del (A2M) NP_000005.2:n.-22_-20del
XM_006719056.2:c.-22_-20del (A2M) XP_006719119.1:n.-22_-20del
NM_000014.5:c.-22_-20del (A2M) NP_000005.2:n.-22_-20del
NM_001347423.1:c.-17-5_-17-3del (A2M) NP_001334352.1:n.-17-5_-17-3del
NM_001347424.1:c.-475_-473del (A2M) NP_001334353.1:n.-475_-473del
NM_001347425.1:c.-312_-310del (A2M) NP_001334354.1:n.-312_-310del
XM_006719056.3:c.-22_-20del (A2M) XP_006719119.1:n.-22_-20del
XM_017018683.1:c.*34-9501_*34-9499del (KLRG1) XP_016874172.1:n.*34-9501_*34-9499del
XM_017018684.1:c.*34-19213_*34-19211del (KLRG1) XP_016874173.1:n.*34-19213_*34-19211del
XM_017018685.1:c.*33+57707_*33+57709del (KLRG1) XP_016874174.1:n.*33+57707_*33+57709del
NM_000014.6:c.-22_-20del (A2M) MANE Select NP_000005.3:n.-22_-20del
NM_001347423.2:c.-17-5_-17-3del (A2M) NP_001334352.2:n.-17-5_-17-3del
NM_001347424.2:c.-475_-473del (A2M) NP_001334353.2:n.-475_-473del
NM_001347425.2:c.-312_-310del (A2M) NP_001334354.2:n.-312_-310del