Canonical Allele Identifier: CA2015347049

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116002T= , CM000674.2:g.9116002T= GRCh38
NC_000012.11:g.9268598T= , CM000674.1:g.9268598T= GRCh37
NC_000012.10:g.9159865T= NCBI36
NG_011717.1:g.4961A=
NG_011717.2:g.4961A=

Transcript Alleles

HGVS Amino-acid change
ENST00000318602.11:c.-153A= (A2M) ENSP00000323929.7:n.-153A=
ENST00000404455.2:c.-18+126A= (A2M) ENSP00000385710.2:n.-18+126A=
ENST00000467091.1:n.60A= (A2M)
ENST00000497324.1:n.16A= (A2M)
NM_000014.5:c.-153A= (A2M) NP_000005.2:n.-153A=
NM_001347423.1:c.-18+126A= (A2M) NP_001334352.1:n.-18+126A=
NM_001347424.1:c.-606A= (A2M) NP_001334353.1:n.-606A=
NM_001347425.1:c.-443A= (A2M) NP_001334354.1:n.-443A=
XM_017018683.1:c.*34-9372T= (KLRG1) XP_016874172.1:n.*34-9372T=
XM_017018684.1:c.*34-19084T= (KLRG1) XP_016874173.1:n.*34-19084T=
XM_017018685.1:c.*33+57836T= (KLRG1) XP_016874174.1:n.*33+57836T=
NM_001347423.2:c.-18+126A= (A2M) NP_001334352.2:n.-18+126A=