Canonical Allele Identifier: CA2015332100

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9079624_9079625delinsCA , CM000674.2:g.9079624_9079625delinsCA GRCh38
NC_000012.11:g.9232220_9232221delinsCA , CM000674.1:g.9232220_9232221delinsCA GRCh37
NC_000012.10:g.9123487_9123488delinsCA NCBI36
NG_011717.1:g.41338_41339delinsTG
NG_011717.2:g.41338_41339delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.12:c.3031+14_3031+15delinsTG (A2M) MANE Select ENSP00000323929.8:n.3031+14_3031+15delinsTG
ENST00000318602.11:c.3031+14_3031+15delinsTG (A2M) ENSP00000323929.7:n.3031+14_3031+15delinsTG
ENST00000542567.1:n.386+14_386+15delinsTG (A2M)
ENST00000543436.2:n.451+10287_451+10288delinsTG (A2M)
ENST00000545828.1:n.349-6904_349-6903delinsTG (A2M)
NM_000014.4:c.3031+14_3031+15delinsTG (A2M) NP_000005.2:n.3031+14_3031+15delinsTG
XM_006719056.2:c.3031+14_3031+15delinsTG (A2M) XP_006719119.1:n.3031+14_3031+15delinsTG
NM_000014.5:c.3031+14_3031+15delinsTG (A2M) NP_000005.2:n.3031+14_3031+15delinsTG
NM_001347423.1:c.3031+14_3031+15delinsTG (A2M) NP_001334352.1:n.3031+14_3031+15delinsTG
NM_001347424.1:c.2731+14_2731+15delinsTG (A2M) NP_001334353.1:n.2731+14_2731+15delinsTG
NM_001347425.1:c.2581+14_2581+15delinsTG (A2M) NP_001334354.1:n.2581+14_2581+15delinsTG
XM_006719056.3:c.3031+14_3031+15delinsTG (A2M) XP_006719119.1:n.3031+14_3031+15delinsTG
XM_017018683.1:c.*33+21458_*33+21459delinsCA (KLRG1) XP_016874172.1:n.*33+21458_*33+21459delinsCA
XM_017018684.1:c.*33+21458_*33+21459delinsCA (KLRG1) XP_016874173.1:n.*33+21458_*33+21459delinsCA
XM_017018685.1:c.*33+21458_*33+21459delinsCA (KLRG1) XP_016874174.1:n.*33+21458_*33+21459delinsCA
NM_000014.6:c.3031+14_3031+15delinsTG (A2M) MANE Select NP_000005.3:n.3031+14_3031+15delinsTG
NM_001347423.2:c.3031+14_3031+15delinsTG (A2M) NP_001334352.2:n.3031+14_3031+15delinsTG
NM_001347424.2:c.2731+14_2731+15delinsTG (A2M) NP_001334353.2:n.2731+14_2731+15delinsTG
NM_001347425.2:c.2581+14_2581+15delinsTG (A2M) NP_001334354.2:n.2581+14_2581+15delinsTG