Canonical Allele Identifier: CA136017446
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs386698546

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29942058_29942060delinsGT , CM000668.2:g.29942058_29942060delinsGT GRCh38
NC_000006.11:g.29909835_29909837delinsGT , CM000668.1:g.29909835_29909837delinsGT GRCh37
NC_000006.10:g.30017814_30017816delinsGT NCBI36
NG_029217.2:g.4593_4595delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000706892.1:n.88_90delinsGT
ENST00000706893.1:c.-189_-187delinsGT ENSP00000516609.1:n.-189_-187delinsGT
ENST00000706894.1:c.-189_-187delinsGT ENSP00000516610.1:n.-189_-187delinsGT
ENST00000706895.1:n.88_90delinsGT
ENST00000706896.1:n.88_90delinsGT
ENST00000706897.1:n.88_90delinsGT
ENST00000706898.1:c.-189_-187delinsGT ENSP00000516611.1:n.-189_-187delinsGT
ENST00000706899.1:n.88_90delinsGT
ENST00000706901.1:c.-189_-187delinsGT ENSP00000516612.1:n.-189_-187delinsGT
ENST00000706902.1:c.-189_-187delinsGT ENSP00000516613.1:n.-189_-187delinsGT
ENST00000706903.1:c.-189_-187delinsGT ENSP00000516614.1:n.-189_-187delinsGT
ENST00000706904.1:c.-189_-187delinsGT ENSP00000516615.1:n.-189_-187delinsGT
ENST00000396634.5:c.-189_-187delinsGT ENSP00000379873.1:n.-189_-187delinsGT