Canonical Allele Identifier: CA2617534876

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116182_9116184del , CM000674.2:g.9116182_9116184del GRCh38
NC_000012.11:g.9268778_9268780del , CM000674.1:g.9268778_9268780del GRCh37
NC_000012.10:g.9160045_9160047del NCBI36
NG_011717.1:g.4780_4782del
NG_011717.2:g.4780_4782del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404455.2:c.-73_-71del (A2M) ENSP00000385710.2:n.-73_-71del
NM_000014.5:c.-334_-332del (A2M) NP_000005.2:n.-334_-332del
NM_001347423.1:c.-73_-71del (A2M) NP_001334352.1:n.-73_-71del
NM_001347424.1:c.-787_-785del (A2M) NP_001334353.1:n.-787_-785del
NM_001347425.1:c.-624_-622del (A2M) NP_001334354.1:n.-624_-622del
XM_017018683.1:c.*34-9192_*34-9190del (KLRG1) XP_016874172.1:n.*34-9192_*34-9190del
XM_017018684.1:c.*34-18904_*34-18902del (KLRG1) XP_016874173.1:n.*34-18904_*34-18902del
XM_017018685.1:c.*33+58016_*33+58018del (KLRG1) XP_016874174.1:n.*33+58016_*33+58018del
NM_001347423.2:c.-73_-71del (A2M) NP_001334352.2:n.-73_-71del