Canonical Allele Identifier: CA2677797289

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945424-TTTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945427_29945429del , CM000668.2:g.29945427_29945429del	GRCh38
NC_000006.11:g.29913204_29913206del , CM000668.1:g.29913204_29913206del	GRCh37
NC_000006.10:g.30021183_30021185del	NCBI36
NG_029217.2:g.7963_7965del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.977-24_977-22del	ENSP00000492789.2:n.977-24_977-22del
ENST00000706892.1:n.2779_2781del
ENST00000706893.1:c.*78-24_*78-22del	ENSP00000516609.1:n.*78-24_*78-22del
ENST00000706894.1:c.*54_*56del	ENSP00000516610.1:n.*54_*56del
ENST00000706895.1:n.2059_2061del
ENST00000706896.1:n.2390-24_2390-22del
ENST00000706897.1:n.1812-24_1812-22del
ENST00000706898.1:c.1112-24_1112-22del	ENSP00000516611.1:n.1112-24_1112-22del
ENST00000706899.1:n.1948-24_1948-22del
ENST00000706900.1:c.1010-24_1010-22del	ENSP00000516617.1:n.1010-24_1010-22del
ENST00000706901.1:c.1094-24_1094-22del	ENSP00000516612.1:n.1094-24_1094-22del
ENST00000706902.1:c.1093+146_1093+148del	ENSP00000516613.1:n.1093+146_1093+148del
ENST00000706903.1:c.1094-24_1094-22del	ENSP00000516614.1:n.1094-24_1094-22del
ENST00000706904.1:c.1093+146_1093+148del	ENSP00000516615.1:n.1093+146_1093+148del
ENST00000706905.1:c.1094-24_1094-22del	ENSP00000516616.1:n.1094-24_1094-22del
ENST00000376809.10:c.1094-24_1094-22del MANE Select	ENSP00000366005.5:n.1094-24_1094-22del
ENST00000376802.2:c.896-24_896-22del	ENSP00000365998.2:n.896-24_896-22del
ENST00000376806.9:c.1112-24_1112-22del	ENSP00000366002.5:n.1112-24_1112-22del
ENST00000376809.9:c.1094-24_1094-22del	ENSP00000366005.5:n.1094-24_1094-22del
ENST00000396634.5:c.1094-24_1094-22del	ENSP00000379873.1:n.1094-24_1094-22del
ENST00000495183.5:n.1333-24_1333-22del
ENST00000496081.5:n.1353-24_1353-22del
NM_002116.7:c.1094-24_1094-22del	NP_002107.3:n.1094-24_1094-22del
NM_002116.8:c.1094-24_1094-22del MANE Select	NP_002107.3:n.1094-24_1094-22del