Canonical Allele Identifier: CA2015347008

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9115928C= , CM000674.2:g.9115928C= GRCh38
NC_000012.11:g.9268524C= , CM000674.1:g.9268524C= GRCh37
NC_000012.10:g.9159791C= NCBI36
NG_011717.1:g.5035G=
NG_011717.2:g.5035G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.11:c.-79G= (A2M) ENSP00000323929.7:n.-79G=
ENST00000404455.2:c.-17-62G= (A2M) ENSP00000385710.2:n.-17-62G=
ENST00000467091.1:n.134G= (A2M)
ENST00000497324.1:n.90G= (A2M)
NM_000014.4:c.-79G= (A2M) NP_000005.2:n.-79G=
XM_006719056.2:c.-79G= (A2M) XP_006719119.1:n.-79G=
NM_000014.5:c.-79G= (A2M) NP_000005.2:n.-79G=
NM_001347423.1:c.-17-62G= (A2M) NP_001334352.1:n.-17-62G=
NM_001347424.1:c.-532G= (A2M) NP_001334353.1:n.-532G=
NM_001347425.1:c.-369G= (A2M) NP_001334354.1:n.-369G=
XM_006719056.3:c.-79G= (A2M) XP_006719119.1:n.-79G=
XM_017018683.1:c.*34-9446C= (KLRG1) XP_016874172.1:n.*34-9446C=
XM_017018684.1:c.*34-19158C= (KLRG1) XP_016874173.1:n.*34-19158C=
XM_017018685.1:c.*33+57762C= (KLRG1) XP_016874174.1:n.*33+57762C=
NM_001347423.2:c.-17-62G= (A2M) NP_001334352.2:n.-17-62G=