Canonical Allele Identifier: CA2015347014

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9115938C= , CM000674.2:g.9115938C= GRCh38
NC_000012.11:g.9268534C= , CM000674.1:g.9268534C= GRCh37
NC_000012.10:g.9159801C= NCBI36
NG_011717.1:g.5025G=
NG_011717.2:g.5025G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.11:c.-89G= (A2M) ENSP00000323929.7:n.-89G=
ENST00000404455.2:c.-17-72G= (A2M) ENSP00000385710.2:n.-17-72G=
ENST00000467091.1:n.124G= (A2M)
ENST00000497324.1:n.80G= (A2M)
NM_000014.4:c.-89G= (A2M) NP_000005.2:n.-89G=
XM_006719056.2:c.-89G= (A2M) XP_006719119.1:n.-89G=
NM_000014.5:c.-89G= (A2M) NP_000005.2:n.-89G=
NM_001347423.1:c.-17-72G= (A2M) NP_001334352.1:n.-17-72G=
NM_001347424.1:c.-542G= (A2M) NP_001334353.1:n.-542G=
NM_001347425.1:c.-379G= (A2M) NP_001334354.1:n.-379G=
XM_006719056.3:c.-89G= (A2M) XP_006719119.1:n.-89G=
XM_017018683.1:c.*34-9436C= (KLRG1) XP_016874172.1:n.*34-9436C=
XM_017018684.1:c.*34-19148C= (KLRG1) XP_016874173.1:n.*34-19148C=
XM_017018685.1:c.*33+57772C= (KLRG1) XP_016874174.1:n.*33+57772C=
NM_001347423.2:c.-17-72G= (A2M) NP_001334352.2:n.-17-72G=