Canonical Allele Identifier: CA2617534591

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9115979_9115980del , CM000674.2:g.9115979_9115980del GRCh38
NC_000012.11:g.9268575_9268576del , CM000674.1:g.9268575_9268576del GRCh37
NC_000012.10:g.9159842_9159843del NCBI36
NG_011717.1:g.4984_4985del
NG_011717.2:g.4984_4985del

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.11:c.-130_-129del (A2M) ENSP00000323929.7:n.-130_-129del
ENST00000404455.2:c.-17-113_-17-112del (A2M) ENSP00000385710.2:n.-17-113_-17-112del
ENST00000467091.1:n.83_84del (A2M)
ENST00000497324.1:n.39_40del (A2M)
NM_000014.5:c.-130_-129del (A2M) NP_000005.2:n.-130_-129del
NM_001347423.1:c.-17-113_-17-112del (A2M) NP_001334352.1:n.-17-113_-17-112del
NM_001347424.1:c.-583_-582del (A2M) NP_001334353.1:n.-583_-582del
NM_001347425.1:c.-420_-419del (A2M) NP_001334354.1:n.-420_-419del
XM_017018683.1:c.*34-9395_*34-9394del (KLRG1) XP_016874172.1:n.*34-9395_*34-9394del
XM_017018684.1:c.*34-19107_*34-19106del (KLRG1) XP_016874173.1:n.*34-19107_*34-19106del
XM_017018685.1:c.*33+57813_*33+57814del (KLRG1) XP_016874174.1:n.*33+57813_*33+57814del
NM_001347423.2:c.-17-113_-17-112del (A2M) NP_001334352.2:n.-17-113_-17-112del