Canonical Allele Identifier: CA2617534638

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9115991del , CM000674.2:g.9115991del GRCh38
NC_000012.11:g.9268587del , CM000674.1:g.9268587del GRCh37
NC_000012.10:g.9159854del NCBI36
NG_011717.1:g.4972del
NG_011717.2:g.4972del

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.11:c.-142del (A2M) ENSP00000323929.7:n.-142del
ENST00000404455.2:c.-17-125del (A2M) ENSP00000385710.2:n.-17-125del
ENST00000467091.1:n.71del (A2M)
ENST00000497324.1:n.27del (A2M)
NM_000014.5:c.-142del (A2M) NP_000005.2:n.-142del
NM_001347423.1:c.-17-125del (A2M) NP_001334352.1:n.-17-125del
NM_001347424.1:c.-595del (A2M) NP_001334353.1:n.-595del
NM_001347425.1:c.-432del (A2M) NP_001334354.1:n.-432del
XM_017018683.1:c.*34-9383del (KLRG1) XP_016874172.1:n.*34-9383del
XM_017018684.1:c.*34-19095del (KLRG1) XP_016874173.1:n.*34-19095del
XM_017018685.1:c.*33+57825del (KLRG1) XP_016874174.1:n.*33+57825del
NM_001347423.2:c.-17-125del (A2M) NP_001334352.2:n.-17-125del