Canonical Allele Identifier: CA2015346979

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9115880G= , CM000674.2:g.9115880G= GRCh38
NC_000012.11:g.9268476G= , CM000674.1:g.9268476G= GRCh37
NC_000012.10:g.9159743G= NCBI36
NG_011717.1:g.5083C=
NG_011717.2:g.5083C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.12:c.-31C= (A2M) MANE Select ENSP00000323929.8:n.-31C=
ENST00000318602.11:c.-31C= (A2M) ENSP00000323929.7:n.-31C=
ENST00000404455.2:c.-17-14C= (A2M) ENSP00000385710.2:n.-17-14C=
ENST00000467091.1:n.182C= (A2M)
ENST00000497324.1:n.138C= (A2M)
NM_000014.4:c.-31C= (A2M) NP_000005.2:n.-31C=
XM_006719056.2:c.-31C= (A2M) XP_006719119.1:n.-31C=
NM_000014.5:c.-31C= (A2M) NP_000005.2:n.-31C=
NM_001347423.1:c.-17-14C= (A2M) NP_001334352.1:n.-17-14C=
NM_001347424.1:c.-484C= (A2M) NP_001334353.1:n.-484C=
NM_001347425.1:c.-321C= (A2M) NP_001334354.1:n.-321C=
XM_006719056.3:c.-31C= (A2M) XP_006719119.1:n.-31C=
XM_017018683.1:c.*34-9494G= (KLRG1) XP_016874172.1:n.*34-9494G=
XM_017018684.1:c.*34-19206G= (KLRG1) XP_016874173.1:n.*34-19206G=
XM_017018685.1:c.*33+57714G= (KLRG1) XP_016874174.1:n.*33+57714G=
NM_000014.6:c.-31C= (A2M) MANE Select NP_000005.3:n.-31C=
NM_001347423.2:c.-17-14C= (A2M) NP_001334352.2:n.-17-14C=
NM_001347424.2:c.-484C= (A2M) NP_001334353.2:n.-484C=
NM_001347425.2:c.-321C= (A2M) NP_001334354.2:n.-321C=