Canonical Allele Identifier: CA693262453

Linked Data

dbSNP Id: rs1271075282

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9068465_9068468del , CM000674.2:g.9068465_9068468del GRCh38
NC_000012.11:g.9221061_9221064del , CM000674.1:g.9221061_9221064del GRCh37
NC_000012.10:g.9112328_9112331del NCBI36
NG_011717.1:g.52501_52504del
NG_011717.2:g.52501_52504del

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.12:c.4367-238_4367-235del (A2M) MANE Select ENSP00000323929.8:n.4367-238_4367-235del
ENST00000318602.11:c.4367-238_4367-235del (A2M) ENSP00000323929.7:n.4367-238_4367-235del
ENST00000495442.1:n.217-238_217-235del (A2M)
ENST00000495709.1:n.340-238_340-235del (A2M)
ENST00000543436.2:n.452-650_452-647del (A2M)
NM_000014.4:c.4367-238_4367-235del (A2M) NP_000005.2:n.4367-238_4367-235del
XM_006719056.2:c.4367-238_4367-235del (A2M) XP_006719119.1:n.4367-238_4367-235del
NM_000014.5:c.4367-238_4367-235del (A2M) NP_000005.2:n.4367-238_4367-235del
NM_001347423.1:c.4367-238_4367-235del (A2M) NP_001334352.1:n.4367-238_4367-235del
NM_001347424.1:c.4067-238_4067-235del (A2M) NP_001334353.1:n.4067-238_4067-235del
NM_001347425.1:c.3917-238_3917-235del (A2M) NP_001334354.1:n.3917-238_3917-235del
XM_006719056.3:c.4367-238_4367-235del (A2M) XP_006719119.1:n.4367-238_4367-235del
XM_017018683.1:c.*33+10299_*33+10302del (KLRG1) XP_016874172.1:n.*33+10299_*33+10302del
XM_017018684.1:c.*33+10299_*33+10302del (KLRG1) XP_016874173.1:n.*33+10299_*33+10302del
XM_017018685.1:c.*33+10299_*33+10302del (KLRG1) XP_016874174.1:n.*33+10299_*33+10302del
NM_000014.6:c.4367-238_4367-235del (A2M) MANE Select NP_000005.3:n.4367-238_4367-235del
NM_001347423.2:c.4367-238_4367-235del (A2M) NP_001334352.2:n.4367-238_4367-235del
NM_001347424.2:c.4067-238_4067-235del (A2M) NP_001334353.2:n.4067-238_4067-235del
NM_001347425.2:c.3917-238_3917-235del (A2M) NP_001334354.2:n.3917-238_3917-235del