Canonical Allele Identifier: CA2015347137

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116191T= , CM000674.2:g.9116191T= GRCh38
NC_000012.11:g.9268787T= , CM000674.1:g.9268787T= GRCh37
NC_000012.10:g.9160054T= NCBI36
NG_011717.1:g.4772A=
NG_011717.2:g.4772A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000404455.2:c.-81A= (A2M) ENSP00000385710.2:n.-81A=
NM_000014.5:c.-342A= (A2M) NP_000005.2:n.-342A=
NM_001347423.1:c.-81A= (A2M) NP_001334352.1:n.-81A=
NM_001347424.1:c.-795A= (A2M) NP_001334353.1:n.-795A=
NM_001347425.1:c.-632A= (A2M) NP_001334354.1:n.-632A=
XM_017018683.1:c.*34-9183T= (KLRG1) XP_016874172.1:n.*34-9183T=
XM_017018684.1:c.*34-18895T= (KLRG1) XP_016874173.1:n.*34-18895T=
XM_017018685.1:c.*33+58025T= (KLRG1) XP_016874174.1:n.*33+58025T=
NM_001347423.2:c.-81A= (A2M) NP_001334352.2:n.-81A=