Canonical Allele Identifier: CA2617528298

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9068624_9068628del , CM000674.2:g.9068624_9068628del GRCh38
NC_000012.11:g.9221220_9221224del , CM000674.1:g.9221220_9221224del GRCh37
NC_000012.10:g.9112487_9112491del NCBI36
NG_011717.1:g.52335_52339del
NG_011717.2:g.52335_52339del

Transcript Alleles

HGVS Amino-acid change
ENST00000318602.12:c.4366+112_4366+116del (A2M) MANE Select ENSP00000323929.8:n.4366+112_4366+116del
ENST00000318602.11:c.4366+112_4366+116del (A2M) ENSP00000323929.7:n.4366+112_4366+116del
ENST00000495442.1:n.216+112_216+116del (A2M)
ENST00000495709.1:n.339+112_339+116del (A2M)
ENST00000543436.2:n.452-816_452-812del (A2M)
NM_000014.4:c.4366+112_4366+116del (A2M) NP_000005.2:n.4366+112_4366+116del
XM_006719056.2:c.4366+112_4366+116del (A2M) XP_006719119.1:n.4366+112_4366+116del
NM_000014.5:c.4366+112_4366+116del (A2M) NP_000005.2:n.4366+112_4366+116del
NM_001347423.1:c.4366+112_4366+116del (A2M) NP_001334352.1:n.4366+112_4366+116del
NM_001347424.1:c.4066+112_4066+116del (A2M) NP_001334353.1:n.4066+112_4066+116del
NM_001347425.1:c.3916+112_3916+116del (A2M) NP_001334354.1:n.3916+112_3916+116del
XM_006719056.3:c.4366+112_4366+116del (A2M) XP_006719119.1:n.4366+112_4366+116del
XM_017018683.1:c.*33+10458_*33+10462del (KLRG1) XP_016874172.1:n.*33+10458_*33+10462del
XM_017018684.1:c.*33+10458_*33+10462del (KLRG1) XP_016874173.1:n.*33+10458_*33+10462del
XM_017018685.1:c.*33+10458_*33+10462del (KLRG1) XP_016874174.1:n.*33+10458_*33+10462del
NM_000014.6:c.4366+112_4366+116del (A2M) MANE Select NP_000005.3:n.4366+112_4366+116del
NM_001347423.2:c.4366+112_4366+116del (A2M) NP_001334352.2:n.4366+112_4366+116del
NM_001347424.2:c.4066+112_4066+116del (A2M) NP_001334353.2:n.4066+112_4066+116del
NM_001347425.2:c.3916+112_3916+116del (A2M) NP_001334354.2:n.3916+112_3916+116del