Canonical Allele Identifier: CA1618522016

Gene: HLA-A

Linked Data

• dbSNP Id: rs1770875731
• gnomAD v3: 6-29942015-ACCTCCATTC-A
• gnomAD v4: 6-29942015-ACCTCCATTC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29942018_29942026del , CM000668.2:g.29942018_29942026del	GRCh38
NC_000006.11:g.29909795_29909803del , CM000668.1:g.29909795_29909803del	GRCh37
NC_000006.10:g.30017774_30017782del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706892.1:n.48_56del
ENST00000706893.1:c.-229_-221del	ENSP00000516609.1:n.-229_-221del
ENST00000706894.1:c.-229_-221del	ENSP00000516610.1:n.-229_-221del
ENST00000706895.1:n.48_56del
ENST00000706896.1:n.48_56del
ENST00000706897.1:n.48_56del
ENST00000706898.1:c.-229_-221del	ENSP00000516611.1:n.-229_-221del
ENST00000706899.1:n.48_56del
ENST00000706901.1:c.-229_-221del	ENSP00000516612.1:n.-229_-221del
ENST00000706902.1:c.-229_-221del	ENSP00000516613.1:n.-229_-221del
ENST00000706903.1:c.-229_-221del	ENSP00000516614.1:n.-229_-221del
ENST00000706904.1:c.-229_-221del	ENSP00000516615.1:n.-229_-221del
ENST00000396634.5:c.-229_-221del	ENSP00000379873.1:n.-229_-221del