Canonical Allele Identifier: CA2677796540

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945220-TTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945222_29945223del , CM000668.2:g.29945222_29945223del	GRCh38
NC_000006.11:g.29912999_29913000del , CM000668.1:g.29912999_29913000del	GRCh37
NC_000006.10:g.30020978_30020979del	NCBI36
NG_029217.2:g.7758_7759del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.929-12_929-11del	ENSP00000492789.2:n.929-12_929-11del
ENST00000706892.1:n.2574_2575del
ENST00000706893.1:c.*30-12_*30-11del	ENSP00000516609.1:n.*30-12_*30-11del
ENST00000706894.1:c.1046-12_1046-11del	ENSP00000516610.1:n.1046-12_1046-11del
ENST00000706895.1:n.1866-12_1866-11del
ENST00000706896.1:n.2342-12_2342-11del
ENST00000706897.1:n.1764-12_1764-11del
ENST00000706898.1:c.1064-12_1064-11del	ENSP00000516611.1:n.1064-12_1064-11del
ENST00000706899.1:n.1900-12_1900-11del
ENST00000706900.1:c.962-12_962-11del	ENSP00000516617.1:n.962-12_962-11del
ENST00000706901.1:c.1046-12_1046-11del	ENSP00000516612.1:n.1046-12_1046-11del
ENST00000706902.1:c.1046-12_1046-11del	ENSP00000516613.1:n.1046-12_1046-11del
ENST00000706903.1:c.1046-12_1046-11del	ENSP00000516614.1:n.1046-12_1046-11del
ENST00000706904.1:c.1046-12_1046-11del	ENSP00000516615.1:n.1046-12_1046-11del
ENST00000706905.1:c.1046-12_1046-11del	ENSP00000516616.1:n.1046-12_1046-11del
ENST00000376809.10:c.1046-12_1046-11del MANE Select	ENSP00000366005.5:n.1046-12_1046-11del
ENST00000638375.1:c.929-12_929-11del	ENSP00000492789.1:n.929-12_929-11del
ENST00000376802.2:c.896-229_896-228del	ENSP00000365998.2:n.896-229_896-228del
ENST00000376806.9:c.1064-12_1064-11del	ENSP00000366002.5:n.1064-12_1064-11del
ENST00000376809.9:c.1046-12_1046-11del	ENSP00000366005.5:n.1046-12_1046-11del
ENST00000396634.5:c.1046-12_1046-11del	ENSP00000379873.1:n.1046-12_1046-11del
ENST00000461903.1:n.1305-12_1305-11del
ENST00000479320.5:n.1287-12_1287-11del
ENST00000495183.5:n.1285-12_1285-11del
ENST00000496081.5:n.1305-12_1305-11del
NM_002116.7:c.1046-12_1046-11del	NP_002107.3:n.1046-12_1046-11del
NM_002116.8:c.1046-12_1046-11del MANE Select	NP_002107.3:n.1046-12_1046-11del