Canonical Allele Identifier: CA2794496562

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116131del , CM000674.2:g.9116131del GRCh38
NC_000012.11:g.9268727del , CM000674.1:g.9268727del GRCh37
NC_000012.10:g.9159994del NCBI36
NG_011717.1:g.4835del
NG_011717.2:g.4835del

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.11:c.-279del (A2M) ENSP00000323929.7:n.-279del
ENST00000404455.2:c.-18del (A2M) ENSP00000385710.2:n.-18del
NM_000014.5:c.-279del (A2M) NP_000005.2:n.-279del
NM_001347423.1:c.-18del (A2M) NP_001334352.1:n.-18del
NM_001347424.1:c.-732del (A2M) NP_001334353.1:n.-732del
NM_001347425.1:c.-569del (A2M) NP_001334354.1:n.-569del
XM_017018683.1:c.*34-9243del (KLRG1) XP_016874172.1:n.*34-9243del
XM_017018684.1:c.*34-18955del (KLRG1) XP_016874173.1:n.*34-18955del
XM_017018685.1:c.*33+57965del (KLRG1) XP_016874174.1:n.*33+57965del
NM_001347423.2:c.-18del (A2M) NP_001334352.2:n.-18del