Canonical Allele Identifier: CA2575099327

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9115927del , CM000674.2:g.9115927del GRCh38
NC_000012.11:g.9268523del , CM000674.1:g.9268523del GRCh37
NC_000012.10:g.9159790del NCBI36
NG_011717.1:g.5037del
NG_011717.2:g.5037del

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.11:c.-77del (A2M) ENSP00000323929.7:n.-77del
ENST00000404455.2:c.-17-60del (A2M) ENSP00000385710.2:n.-17-60del
ENST00000467091.1:n.136del (A2M)
ENST00000497324.1:n.92del (A2M)
NM_000014.4:c.-77del (A2M) NP_000005.2:n.-77del
XM_006719056.2:c.-77del (A2M) XP_006719119.1:n.-77del
NM_000014.5:c.-77del (A2M) NP_000005.2:n.-77del
NM_001347423.1:c.-17-60del (A2M) NP_001334352.1:n.-17-60del
NM_001347424.1:c.-530del (A2M) NP_001334353.1:n.-530del
NM_001347425.1:c.-367del (A2M) NP_001334354.1:n.-367del
XM_006719056.3:c.-77del (A2M) XP_006719119.1:n.-77del
XM_017018683.1:c.*34-9447del (KLRG1) XP_016874172.1:n.*34-9447del
XM_017018684.1:c.*34-19159del (KLRG1) XP_016874173.1:n.*34-19159del
XM_017018685.1:c.*33+57761del (KLRG1) XP_016874174.1:n.*33+57761del
NM_001347423.2:c.-17-60del (A2M) NP_001334352.2:n.-17-60del