Canonical Allele Identifier: CA2617534643

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9115996dup , CM000674.2:g.9115996dup GRCh38
NC_000012.11:g.9268592dup , CM000674.1:g.9268592dup GRCh37
NC_000012.10:g.9159859dup NCBI36
NG_011717.1:g.4969dup
NG_011717.2:g.4969dup

Transcript Alleles

HGVS Amino-acid change
ENST00000318602.11:c.-145dup (A2M) ENSP00000323929.7:n.-145dup
ENST00000404455.2:c.-17-128dup (A2M) ENSP00000385710.2:n.-17-128dup
ENST00000467091.1:n.68dup (A2M)
ENST00000497324.1:n.24dup (A2M)
NM_000014.5:c.-145dup (A2M) NP_000005.2:n.-145dup
NM_001347423.1:c.-17-128dup (A2M) NP_001334352.1:n.-17-128dup
NM_001347424.1:c.-598dup (A2M) NP_001334353.1:n.-598dup
NM_001347425.1:c.-435dup (A2M) NP_001334354.1:n.-435dup
XM_017018683.1:c.*34-9378dup (KLRG1) XP_016874172.1:n.*34-9378dup
XM_017018684.1:c.*34-19090dup (KLRG1) XP_016874173.1:n.*34-19090dup
XM_017018685.1:c.*33+57830dup (KLRG1) XP_016874174.1:n.*33+57830dup
NM_001347423.2:c.-17-128dup (A2M) NP_001334352.2:n.-17-128dup