Canonical Allele Identifier: CA2617534631

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9115992_9115993del , CM000674.2:g.9115992_9115993del GRCh38
NC_000012.11:g.9268588_9268589del , CM000674.1:g.9268588_9268589del GRCh37
NC_000012.10:g.9159855_9159856del NCBI36
NG_011717.1:g.4973_4974del
NG_011717.2:g.4973_4974del

Transcript Alleles

HGVS Amino-acid change
ENST00000318602.11:c.-141_-140del (A2M) ENSP00000323929.7:n.-141_-140del
ENST00000404455.2:c.-17-124_-17-123del (A2M) ENSP00000385710.2:n.-17-124_-17-123del
ENST00000467091.1:n.72_73del (A2M)
ENST00000497324.1:n.28_29del (A2M)
NM_000014.5:c.-141_-140del (A2M) NP_000005.2:n.-141_-140del
NM_001347423.1:c.-17-124_-17-123del (A2M) NP_001334352.1:n.-17-124_-17-123del
NM_001347424.1:c.-594_-593del (A2M) NP_001334353.1:n.-594_-593del
NM_001347425.1:c.-431_-430del (A2M) NP_001334354.1:n.-431_-430del
XM_017018683.1:c.*34-9382_*34-9381del (KLRG1) XP_016874172.1:n.*34-9382_*34-9381del
XM_017018684.1:c.*34-19094_*34-19093del (KLRG1) XP_016874173.1:n.*34-19094_*34-19093del
XM_017018685.1:c.*33+57826_*33+57827del (KLRG1) XP_016874174.1:n.*33+57826_*33+57827del
NM_001347423.2:c.-17-124_-17-123del (A2M) NP_001334352.2:n.-17-124_-17-123del