Canonical Allele Identifier: CA2677793749
Gene: HLA-A HGNC NCBI

Linked Data

gnomAD v4: 6-29942127-AGGG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29942128_29942130del , CM000668.2:g.29942128_29942130del GRCh38
NC_000006.11:g.29909905_29909907del , CM000668.1:g.29909905_29909907del GRCh37
NC_000006.10:g.30017884_30017886del NCBI36
NG_029217.2:g.4663_4665del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706892.1:n.126+32_126+34del
ENST00000706893.1:c.-151+32_-151+34del ENSP00000516609.1:n.-151+32_-151+34del
ENST00000706894.1:c.-151+32_-151+34del ENSP00000516610.1:n.-151+32_-151+34del
ENST00000706895.1:n.126+32_126+34del
ENST00000706896.1:n.126+32_126+34del
ENST00000706897.1:n.126+32_126+34del
ENST00000706898.1:c.-151+32_-151+34del ENSP00000516611.1:n.-151+32_-151+34del
ENST00000706899.1:n.126+32_126+34del
ENST00000706901.1:c.-151+32_-151+34del ENSP00000516612.1:n.-151+32_-151+34del
ENST00000706902.1:c.-151+32_-151+34del ENSP00000516613.1:n.-151+32_-151+34del
ENST00000706903.1:c.-151+32_-151+34del ENSP00000516614.1:n.-151+32_-151+34del
ENST00000706904.1:c.-151+32_-151+34del ENSP00000516615.1:n.-151+32_-151+34del
ENST00000396634.5:c.-151+32_-151+34del ENSP00000379873.1:n.-151+32_-151+34del
ENST00000429656.1:n.938_940del
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