Canonical Allele Identifier: CA2015347081

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116095T= , CM000674.2:g.9116095T= GRCh38
NC_000012.11:g.9268691T= , CM000674.1:g.9268691T= GRCh37
NC_000012.10:g.9159958T= NCBI36
NG_011717.1:g.4868A=
NG_011717.2:g.4868A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.11:c.-246A= (A2M) ENSP00000323929.7:n.-246A=
ENST00000404455.2:c.-18+33A= (A2M) ENSP00000385710.2:n.-18+33A=
NM_000014.5:c.-246A= (A2M) NP_000005.2:n.-246A=
NM_001347423.1:c.-18+33A= (A2M) NP_001334352.1:n.-18+33A=
NM_001347424.1:c.-699A= (A2M) NP_001334353.1:n.-699A=
NM_001347425.1:c.-536A= (A2M) NP_001334354.1:n.-536A=
XM_017018683.1:c.*34-9279T= (KLRG1) XP_016874172.1:n.*34-9279T=
XM_017018684.1:c.*34-18991T= (KLRG1) XP_016874173.1:n.*34-18991T=
XM_017018685.1:c.*33+57929T= (KLRG1) XP_016874174.1:n.*33+57929T=
NM_001347423.2:c.-18+33A= (A2M) NP_001334352.2:n.-18+33A=