Canonical Allele Identifier: CA2015346882

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9115670T= , CM000674.2:g.9115670T= GRCh38
NC_000012.11:g.9268266T= , CM000674.1:g.9268266T= GRCh37
NC_000012.10:g.9159533T= NCBI36
NG_011717.1:g.5293A=
NG_011717.2:g.5293A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.12:c.86+94A= (A2M) MANE Select ENSP00000323929.8:n.86+94A=
ENST00000318602.11:c.86+94A= (A2M) ENSP00000323929.7:n.86+94A=
ENST00000404455.2:c.86+94A= (A2M) ENSP00000385710.2:n.86+94A=
ENST00000467091.1:n.298+94A= (A2M)
ENST00000497324.1:n.254+94A= (A2M)
ENST00000539638.5:c.86+94A= (A2M) ENSP00000445717.1:n.86+94A=
NM_000014.4:c.86+94A= (A2M) NP_000005.2:n.86+94A=
XM_006719056.2:c.86+94A= (A2M) XP_006719119.1:n.86+94A=
NM_000014.5:c.86+94A= (A2M) NP_000005.2:n.86+94A=
NM_001347423.1:c.86+94A= (A2M) NP_001334352.1:n.86+94A=
NM_001347424.1:c.-368+94A= (A2M) NP_001334353.1:n.-368+94A=
NM_001347425.1:c.-205+94A= (A2M) NP_001334354.1:n.-205+94A=
XM_006719056.3:c.86+94A= (A2M) XP_006719119.1:n.86+94A=
XM_017018683.1:c.*34-9704T= (KLRG1) XP_016874172.1:n.*34-9704T=
XM_017018684.1:c.*34-19416T= (KLRG1) XP_016874173.1:n.*34-19416T=
XM_017018685.1:c.*33+57504T= (KLRG1) XP_016874174.1:n.*33+57504T=
NM_000014.6:c.86+94A= (A2M) MANE Select NP_000005.3:n.86+94A=
NM_001347423.2:c.86+94A= (A2M) NP_001334352.2:n.86+94A=
NM_001347424.2:c.-368+94A= (A2M) NP_001334353.2:n.-368+94A=
NM_001347425.2:c.-205+94A= (A2M) NP_001334354.2:n.-205+94A=