Canonical Allele Identifier: CA2015347084

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116106T= , CM000674.2:g.9116106T= GRCh38
NC_000012.11:g.9268702T= , CM000674.1:g.9268702T= GRCh37
NC_000012.10:g.9159969T= NCBI36
NG_011717.1:g.4857A=
NG_011717.2:g.4857A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.11:c.-257A= (A2M) ENSP00000323929.7:n.-257A=
ENST00000404455.2:c.-18+22A= (A2M) ENSP00000385710.2:n.-18+22A=
NM_000014.5:c.-257A= (A2M) NP_000005.2:n.-257A=
NM_001347423.1:c.-18+22A= (A2M) NP_001334352.1:n.-18+22A=
NM_001347424.1:c.-710A= (A2M) NP_001334353.1:n.-710A=
NM_001347425.1:c.-547A= (A2M) NP_001334354.1:n.-547A=
XM_017018683.1:c.*34-9268T= (KLRG1) XP_016874172.1:n.*34-9268T=
XM_017018684.1:c.*34-18980T= (KLRG1) XP_016874173.1:n.*34-18980T=
XM_017018685.1:c.*33+57940T= (KLRG1) XP_016874174.1:n.*33+57940T=
NM_001347423.2:c.-18+22A= (A2M) NP_001334352.2:n.-18+22A=