Canonical Allele Identifier: CA2015347043

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9115983A= , CM000674.2:g.9115983A= GRCh38
NC_000012.11:g.9268579A= , CM000674.1:g.9268579A= GRCh37
NC_000012.10:g.9159846A= NCBI36
NG_011717.1:g.4980T=
NG_011717.2:g.4980T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.11:c.-134T= (A2M) ENSP00000323929.7:n.-134T=
ENST00000404455.2:c.-17-117T= (A2M) ENSP00000385710.2:n.-17-117T=
ENST00000467091.1:n.79T= (A2M)
ENST00000497324.1:n.35T= (A2M)
NM_000014.5:c.-134T= (A2M) NP_000005.2:n.-134T=
NM_001347423.1:c.-17-117T= (A2M) NP_001334352.1:n.-17-117T=
NM_001347424.1:c.-587T= (A2M) NP_001334353.1:n.-587T=
NM_001347425.1:c.-424T= (A2M) NP_001334354.1:n.-424T=
XM_017018683.1:c.*34-9391A= (KLRG1) XP_016874172.1:n.*34-9391A=
XM_017018684.1:c.*34-19103A= (KLRG1) XP_016874173.1:n.*34-19103A=
XM_017018685.1:c.*33+57817A= (KLRG1) XP_016874174.1:n.*33+57817A=
NM_001347423.2:c.-17-117T= (A2M) NP_001334352.2:n.-17-117T=