Canonical Allele Identifier: CA2617534914

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116204del , CM000674.2:g.9116204del GRCh38
NC_000012.11:g.9268800del , CM000674.1:g.9268800del GRCh37
NC_000012.10:g.9160067del NCBI36
NG_011717.1:g.4762del
NG_011717.2:g.4762del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404455.2:c.-91del (A2M) ENSP00000385710.2:n.-91del
NM_000014.5:c.-352del (A2M) NP_000005.2:n.-352del
NM_001347423.1:c.-91del (A2M) NP_001334352.1:n.-91del
NM_001347424.1:c.-805del (A2M) NP_001334353.1:n.-805del
NM_001347425.1:c.-642del (A2M) NP_001334354.1:n.-642del
XM_017018683.1:c.*34-9170del (KLRG1) XP_016874172.1:n.*34-9170del
XM_017018684.1:c.*34-18882del (KLRG1) XP_016874173.1:n.*34-18882del
XM_017018685.1:c.*33+58038del (KLRG1) XP_016874174.1:n.*33+58038del
NM_001347423.2:c.-91del (A2M) NP_001334352.2:n.-91del