Canonical Allele Identifier: CA2015347132

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116185A= , CM000674.2:g.9116185A= GRCh38
NC_000012.11:g.9268781A= , CM000674.1:g.9268781A= GRCh37
NC_000012.10:g.9160048A= NCBI36
NG_011717.1:g.4778T=
NG_011717.2:g.4778T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000404455.2:c.-75T= (A2M) ENSP00000385710.2:n.-75T=
NM_000014.5:c.-336T= (A2M) NP_000005.2:n.-336T=
NM_001347423.1:c.-75T= (A2M) NP_001334352.1:n.-75T=
NM_001347424.1:c.-789T= (A2M) NP_001334353.1:n.-789T=
NM_001347425.1:c.-626T= (A2M) NP_001334354.1:n.-626T=
XM_017018683.1:c.*34-9189A= (KLRG1) XP_016874172.1:n.*34-9189A=
XM_017018684.1:c.*34-18901A= (KLRG1) XP_016874173.1:n.*34-18901A=
XM_017018685.1:c.*33+58019A= (KLRG1) XP_016874174.1:n.*33+58019A=
NM_001347423.2:c.-75T= (A2M) NP_001334352.2:n.-75T=