Canonical Allele Identifier: CA2015346990

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9115903A= , CM000674.2:g.9115903A= GRCh38
NC_000012.11:g.9268499A= , CM000674.1:g.9268499A= GRCh37
NC_000012.10:g.9159766A= NCBI36
NG_011717.1:g.5060T=
NG_011717.2:g.5060T=

Transcript Alleles

HGVS Amino-acid change
ENST00000318602.12:c.-54T= (A2M) MANE Select ENSP00000323929.8:n.-54T=
ENST00000318602.11:c.-54T= (A2M) ENSP00000323929.7:n.-54T=
ENST00000404455.2:c.-17-37T= (A2M) ENSP00000385710.2:n.-17-37T=
ENST00000467091.1:n.159T= (A2M)
ENST00000497324.1:n.115T= (A2M)
NM_000014.4:c.-54T= (A2M) NP_000005.2:n.-54T=
XM_006719056.2:c.-54T= (A2M) XP_006719119.1:n.-54T=
NM_000014.5:c.-54T= (A2M) NP_000005.2:n.-54T=
NM_001347423.1:c.-17-37T= (A2M) NP_001334352.1:n.-17-37T=
NM_001347424.1:c.-507T= (A2M) NP_001334353.1:n.-507T=
NM_001347425.1:c.-344T= (A2M) NP_001334354.1:n.-344T=
XM_006719056.3:c.-54T= (A2M) XP_006719119.1:n.-54T=
XM_017018683.1:c.*34-9471A= (KLRG1) XP_016874172.1:n.*34-9471A=
XM_017018684.1:c.*34-19183A= (KLRG1) XP_016874173.1:n.*34-19183A=
XM_017018685.1:c.*33+57737A= (KLRG1) XP_016874174.1:n.*33+57737A=
NM_000014.6:c.-54T= (A2M) MANE Select NP_000005.3:n.-54T=
NM_001347423.2:c.-17-37T= (A2M) NP_001334352.2:n.-17-37T=
NM_001347424.2:c.-507T= (A2M) NP_001334353.2:n.-507T=
NM_001347425.2:c.-344T= (A2M) NP_001334354.2:n.-344T=