Canonical Allele Identifier: CA2015327695

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9068924_9068925delinsTG , CM000674.2:g.9068924_9068925delinsTG GRCh38
NC_000012.11:g.9221520_9221521delinsTG , CM000674.1:g.9221520_9221521delinsTG GRCh37
NC_000012.10:g.9112787_9112788delinsTG NCBI36
NG_011717.1:g.52038_52039delinsCA
NG_011717.2:g.52038_52039delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.12:c.4264-83_4264-82delinsCA (A2M) MANE Select ENSP00000323929.8:n.4264-83_4264-82delinsCA
ENST00000318602.11:c.4264-83_4264-82delinsCA (A2M) ENSP00000323929.7:n.4264-83_4264-82delinsCA
ENST00000495442.1:n.31_32delinsCA (A2M)
ENST00000495709.1:n.154_155delinsCA (A2M)
ENST00000543436.2:n.452-1113_452-1112delinsCA (A2M)
NM_000014.4:c.4264-83_4264-82delinsCA (A2M) NP_000005.2:n.4264-83_4264-82delinsCA
XM_006719056.2:c.4264-83_4264-82delinsCA (A2M) XP_006719119.1:n.4264-83_4264-82delinsCA
NM_000014.5:c.4264-83_4264-82delinsCA (A2M) NP_000005.2:n.4264-83_4264-82delinsCA
NM_001347423.1:c.4264-83_4264-82delinsCA (A2M) NP_001334352.1:n.4264-83_4264-82delinsCA
NM_001347424.1:c.3964-83_3964-82delinsCA (A2M) NP_001334353.1:n.3964-83_3964-82delinsCA
NM_001347425.1:c.3814-83_3814-82delinsCA (A2M) NP_001334354.1:n.3814-83_3814-82delinsCA
XM_006719056.3:c.4264-83_4264-82delinsCA (A2M) XP_006719119.1:n.4264-83_4264-82delinsCA
XM_017018683.1:c.*33+10758_*33+10759delinsTG (KLRG1) XP_016874172.1:n.*33+10758_*33+10759delinsTG
XM_017018684.1:c.*33+10758_*33+10759delinsTG (KLRG1) XP_016874173.1:n.*33+10758_*33+10759delinsTG
XM_017018685.1:c.*33+10758_*33+10759delinsTG (KLRG1) XP_016874174.1:n.*33+10758_*33+10759delinsTG
NM_000014.6:c.4264-83_4264-82delinsCA (A2M) MANE Select NP_000005.3:n.4264-83_4264-82delinsCA
NM_001347423.2:c.4264-83_4264-82delinsCA (A2M) NP_001334352.2:n.4264-83_4264-82delinsCA
NM_001347424.2:c.3964-83_3964-82delinsCA (A2M) NP_001334353.2:n.3964-83_3964-82delinsCA
NM_001347425.2:c.3814-83_3814-82delinsCA (A2M) NP_001334354.2:n.3814-83_3814-82delinsCA