Canonical Allele Identifier: CA2015347054

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116013G= , CM000674.2:g.9116013G= GRCh38
NC_000012.11:g.9268609G= , CM000674.1:g.9268609G= GRCh37
NC_000012.10:g.9159876G= NCBI36
NG_011717.1:g.4950C=
NG_011717.2:g.4950C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.11:c.-164C= (A2M) ENSP00000323929.7:n.-164C=
ENST00000404455.2:c.-18+115C= (A2M) ENSP00000385710.2:n.-18+115C=
ENST00000467091.1:n.49C= (A2M)
ENST00000497324.1:n.5C= (A2M)
NM_000014.5:c.-164C= (A2M) NP_000005.2:n.-164C=
NM_001347423.1:c.-18+115C= (A2M) NP_001334352.1:n.-18+115C=
NM_001347424.1:c.-617C= (A2M) NP_001334353.1:n.-617C=
NM_001347425.1:c.-454C= (A2M) NP_001334354.1:n.-454C=
XM_017018683.1:c.*34-9361G= (KLRG1) XP_016874172.1:n.*34-9361G=
XM_017018684.1:c.*34-19073G= (KLRG1) XP_016874173.1:n.*34-19073G=
XM_017018685.1:c.*33+57847G= (KLRG1) XP_016874174.1:n.*33+57847G=
NM_001347423.2:c.-18+115C= (A2M) NP_001334352.2:n.-18+115C=