Canonical Allele Identifier: CA2677794951

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29944618-T-TGA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944619_29944620insAG , CM000668.2:g.29944619_29944620insAG	GRCh38
NC_000006.11:g.29912396_29912397insAG , CM000668.1:g.29912396_29912397insAG	GRCh37
NC_000006.10:g.30020375_30020376insAG	NCBI36
NG_029217.2:g.7155_7156insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.895+222_895+223insAG	ENSP00000492789.2:n.895+222_895+223insAG
ENST00000706892.1:n.1971_1972insAG
ENST00000706893.1:c.1049_1050insAG	ENSP00000516609.1:p.Trp350Ter
ENST00000706894.1:c.1012+3_1012+4insAG	ENSP00000516610.1:n.1012+3_1012+4insAG
ENST00000706895.1:n.1393_1394insAG
ENST00000706896.1:n.1869_1870insAG
ENST00000706897.1:n.1291_1292insAG
ENST00000706898.1:c.1015_1016insAG	ENSP00000516611.1:p.Gly339GlufsTer5
ENST00000706899.1:n.1866+3_1866+4insAG
ENST00000706900.1:c.928+3_928+4insAG	ENSP00000516617.1:n.928+3_928+4insAG
ENST00000706901.1:c.1012+3_1012+4insAG	ENSP00000516612.1:n.1012+3_1012+4insAG
ENST00000706902.1:c.1012+3_1012+4insAG	ENSP00000516613.1:n.1012+3_1012+4insAG
ENST00000706903.1:c.1012+3_1012+4insAG	ENSP00000516614.1:n.1012+3_1012+4insAG
ENST00000706904.1:c.1012+3_1012+4insAG	ENSP00000516615.1:n.1012+3_1012+4insAG
ENST00000706905.1:c.1012+3_1012+4insAG	ENSP00000516616.1:n.1012+3_1012+4insAG
ENST00000376809.10:c.1012+3_1012+4insAG MANE Select	ENSP00000366005.5:n.1012+3_1012+4insAG
ENST00000638375.1:c.895+222_895+223insAG	ENSP00000492789.1:n.895+222_895+223insAG
ENST00000376802.2:c.895+222_895+223insAG	ENSP00000365998.2:n.895+222_895+223insAG
ENST00000376806.9:c.1015_1016insAG	ENSP00000366002.5:p.Gly339GlufsTer5
ENST00000376809.9:c.1012+3_1012+4insAG	ENSP00000366005.5:n.1012+3_1012+4insAG
ENST00000396634.5:c.1012+3_1012+4insAG	ENSP00000379873.1:n.1012+3_1012+4insAG
ENST00000461903.1:n.1256_1257insAG
ENST00000479320.5:n.1253+3_1253+4insAG
ENST00000495183.5:n.1255+3_1255+4insAG
ENST00000496081.5:n.832_833insAG
NM_002116.7:c.1012+3_1012+4insAG	NP_002107.3:n.1012+3_1012+4insAG
NM_002116.8:c.1012+3_1012+4insAG MANE Select	NP_002107.3:n.1012+3_1012+4insAG