Canonical Allele Identifier: CA2015347051

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116003T= , CM000674.2:g.9116003T= GRCh38
NC_000012.11:g.9268599T= , CM000674.1:g.9268599T= GRCh37
NC_000012.10:g.9159866T= NCBI36
NG_011717.1:g.4960A=
NG_011717.2:g.4960A=

Transcript Alleles

HGVS Amino-acid change
ENST00000318602.11:c.-154A= (A2M) ENSP00000323929.7:n.-154A=
ENST00000404455.2:c.-18+125A= (A2M) ENSP00000385710.2:n.-18+125A=
ENST00000467091.1:n.59A= (A2M)
ENST00000497324.1:n.15A= (A2M)
NM_000014.5:c.-154A= (A2M) NP_000005.2:n.-154A=
NM_001347423.1:c.-18+125A= (A2M) NP_001334352.1:n.-18+125A=
NM_001347424.1:c.-607A= (A2M) NP_001334353.1:n.-607A=
NM_001347425.1:c.-444A= (A2M) NP_001334354.1:n.-444A=
XM_017018683.1:c.*34-9371T= (KLRG1) XP_016874172.1:n.*34-9371T=
XM_017018684.1:c.*34-19083T= (KLRG1) XP_016874173.1:n.*34-19083T=
XM_017018685.1:c.*33+57837T= (KLRG1) XP_016874174.1:n.*33+57837T=
NM_001347423.2:c.-18+125A= (A2M) NP_001334352.2:n.-18+125A=