Canonical Allele Identifier: CA2677794784

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29944568-ATCACTGGAGCTGTGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944571_29944585del , CM000668.2:g.29944571_29944585del	GRCh38
NC_000006.11:g.29912348_29912362del , CM000668.1:g.29912348_29912362del	GRCh37
NC_000006.10:g.30020327_30020341del	NCBI36
NG_029217.2:g.7107_7121del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.895+174_895+188del	ENSP00000492789.2:n.895+174_895+188del
ENST00000706892.1:n.1923_1937del
ENST00000706893.1:c.1001_1015del	ENSP00000516609.1:p.His334_Gly338del
ENST00000706894.1:c.967_981del	ENSP00000516610.1:p.Thr323_Val327del
ENST00000706895.1:n.1345_1359del
ENST00000706896.1:n.1821_1835del
ENST00000706897.1:n.1243_1257del
ENST00000706898.1:c.967_981del	ENSP00000516611.1:p.Thr323_Val327del
ENST00000706899.1:n.1821_1835del
ENST00000706900.1:c.883_897del	ENSP00000516617.1:p.Thr295_Val299del
ENST00000706901.1:c.967_981del	ENSP00000516612.1:p.Thr323_Val327del
ENST00000706902.1:c.967_981del	ENSP00000516613.1:p.Thr323_Val327del
ENST00000706903.1:c.967_981del	ENSP00000516614.1:p.Thr323_Val327del
ENST00000706904.1:c.967_981del	ENSP00000516615.1:p.Thr323_Val327del
ENST00000706905.1:c.967_981del	ENSP00000516616.1:p.Thr323_Val327del
ENST00000376809.10:c.967_981del MANE Select	ENSP00000366005.5:p.Thr323_Val327del
ENST00000638375.1:c.895+174_895+188del	ENSP00000492789.1:n.895+174_895+188del
ENST00000376802.2:c.895+174_895+188del	ENSP00000365998.2:n.895+174_895+188del
ENST00000376806.9:c.967_981del	ENSP00000366002.5:p.Thr323_Val327del
ENST00000376809.9:c.967_981del	ENSP00000366005.5:p.Thr323_Val327del
ENST00000396634.5:c.967_981del	ENSP00000379873.1:p.Thr323_Val327del
ENST00000461903.1:n.1208_1222del
ENST00000479320.5:n.1208_1222del
ENST00000495183.5:n.1210_1224del
ENST00000496081.5:n.784_798del
NM_002116.7:c.967_981del	NP_002107.3:p.Thr323_Val327del
NM_002116.8:c.967_981del MANE Select	NP_002107.3:p.Thr323_Val327del