Canonical Allele Identifier: CA2617534709

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116042del , CM000674.2:g.9116042del GRCh38
NC_000012.11:g.9268638del , CM000674.1:g.9268638del GRCh37
NC_000012.10:g.9159905del NCBI36
NG_011717.1:g.4922del
NG_011717.2:g.4922del

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.11:c.-192del (A2M) ENSP00000323929.7:n.-192del
ENST00000404455.2:c.-18+87del (A2M) ENSP00000385710.2:n.-18+87del
ENST00000467091.1:n.21del (A2M)
NM_000014.5:c.-192del (A2M) NP_000005.2:n.-192del
NM_001347423.1:c.-18+87del (A2M) NP_001334352.1:n.-18+87del
NM_001347424.1:c.-645del (A2M) NP_001334353.1:n.-645del
NM_001347425.1:c.-482del (A2M) NP_001334354.1:n.-482del
XM_017018683.1:c.*34-9332del (KLRG1) XP_016874172.1:n.*34-9332del
XM_017018684.1:c.*34-19044del (KLRG1) XP_016874173.1:n.*34-19044del
XM_017018685.1:c.*33+57876del (KLRG1) XP_016874174.1:n.*33+57876del
NM_001347423.2:c.-18+87del (A2M) NP_001334352.2:n.-18+87del