Canonical Allele Identifier: CA2677795111

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29944714-C-CTTTTCTTTGAATAGATT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944714_29944715insTTTTCTTTGAATAGATT , CM000668.2:g.29944714_29944715insTTTTCTTTGAATAGATT	GRCh38
NC_000006.11:g.29912491_29912492insTTTTCTTTGAATAGATT , CM000668.1:g.29912491_29912492insTTTTCTTTGAATAGATT	GRCh37
NC_000006.10:g.30020470_30020471insTTTTCTTTGAATAGATT	NCBI36
NG_029217.2:g.7250_7251insTTTTCTTTGAATAGATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.895+317_895+318insTTTTCTTTGAATAGATT	ENSP00000492789.2:n.895+317_895+318insTTTTCTTTGAATAGATT
ENST00000706892.1:n.2066_2067insTTTTCTTTGAATAGATT
ENST00000706893.1:c.1064+80_1064+81insTTTTCTTTGAATAGATT	ENSP00000516609.1:n.1064+80_1064+81insTTTTCTTTGAATAGATT
ENST00000706894.1:c.1012+98_1012+99insTTTTCTTTGAATAGATT	ENSP00000516610.1:n.1012+98_1012+99insTTTTCTTTGAATAGATT
ENST00000706895.1:n.1488_1489insTTTTCTTTGAATAGATT
ENST00000706896.1:n.1964_1965insTTTTCTTTGAATAGATT
ENST00000706897.1:n.1386_1387insTTTTCTTTGAATAGATT
ENST00000706898.1:c.1030+80_1030+81insTTTTCTTTGAATAGATT	ENSP00000516611.1:n.1030+80_1030+81insTTTTCTTTGAATAGATT
ENST00000706899.1:n.1866+98_1866+99insTTTTCTTTGAATAGATT
ENST00000706900.1:c.928+98_928+99insTTTTCTTTGAATAGATT	ENSP00000516617.1:n.928+98_928+99insTTTTCTTTGAATAGATT
ENST00000706901.1:c.1012+98_1012+99insTTTTCTTTGAATAGATT	ENSP00000516612.1:n.1012+98_1012+99insTTTTCTTTGAATAGATT
ENST00000706902.1:c.1012+98_1012+99insTTTTCTTTGAATAGATT	ENSP00000516613.1:n.1012+98_1012+99insTTTTCTTTGAATAGATT
ENST00000706903.1:c.1012+98_1012+99insTTTTCTTTGAATAGATT	ENSP00000516614.1:n.1012+98_1012+99insTTTTCTTTGAATAGATT
ENST00000706904.1:c.1012+98_1012+99insTTTTCTTTGAATAGATT	ENSP00000516615.1:n.1012+98_1012+99insTTTTCTTTGAATAGATT
ENST00000706905.1:c.1012+98_1012+99insTTTTCTTTGAATAGATT	ENSP00000516616.1:n.1012+98_1012+99insTTTTCTTTGAATAGATT
ENST00000376809.10:c.1012+98_1012+99insTTTTCTTTGAATAGATT MANE Select	ENSP00000366005.5:n.1012+98_1012+99insTTTTCTTTGAATAGATT
ENST00000638375.1:c.895+317_895+318insTTTTCTTTGAATAGATT	ENSP00000492789.1:n.895+317_895+318insTTTTCTTTGAATAGATT
ENST00000376802.2:c.895+317_895+318insTTTTCTTTGAATAGATT	ENSP00000365998.2:n.895+317_895+318insTTTTCTTTGAATAGATT
ENST00000376806.9:c.1030+80_1030+81insTTTTCTTTGAATAGATT	ENSP00000366002.5:n.1030+80_1030+81insTTTTCTTTGAATAGATT
ENST00000376809.9:c.1012+98_1012+99insTTTTCTTTGAATAGATT	ENSP00000366005.5:n.1012+98_1012+99insTTTTCTTTGAATAGATT
ENST00000396634.5:c.1012+98_1012+99insTTTTCTTTGAATAGATT	ENSP00000379873.1:n.1012+98_1012+99insTTTTCTTTGAATAGATT
ENST00000461903.1:n.1271+80_1271+81insTTTTCTTTGAATAGATT
ENST00000479320.5:n.1253+98_1253+99insTTTTCTTTGAATAGATT
ENST00000495183.5:n.1255+98_1255+99insTTTTCTTTGAATAGATT
ENST00000496081.5:n.927_928insTTTTCTTTGAATAGATT
NM_002116.7:c.1012+98_1012+99insTTTTCTTTGAATAGATT	NP_002107.3:n.1012+98_1012+99insTTTTCTTTGAATAGATT
NM_002116.8:c.1012+98_1012+99insTTTTCTTTGAATAGATT MANE Select	NP_002107.3:n.1012+98_1012+99insTTTTCTTTGAATAGATT