Canonical Allele Identifier: CA566285974

Gene: HLA-A

Linked Data

• dbSNP Id: rs1415242728
• gnomAD v2: 6-29910333-G-GGT
• MyVariant Identifiers: chr6:g.29910335delinsTGC (hg19) ; chr6:g.29910333_29910334insGT (hg19) ; chr6:g.29942558delinsTGC (hg38) ; chr6:g.29942556_29942557insGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29942557_29942558insTG , CM000668.2:g.29942557_29942558insTG	GRCh38
NC_000006.11:g.29910334_29910335insTG , CM000668.1:g.29910334_29910335insTG	GRCh37
NC_000006.10:g.30018313_30018314insTG	NCBI36
NG_029217.2:g.5092_5093insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.4_5insTG	ENSP00000492789.2:p.Ala2ValfsTer19
ENST00000706892.1:n.280_281insTG
ENST00000706893.1:c.4_5insTG	ENSP00000516609.1:p.Ala2ValfsTer19
ENST00000706894.1:c.4_5insTG	ENSP00000516610.1:p.Ala2ValfsTer19
ENST00000706895.1:n.280_281insTG
ENST00000706896.1:n.280_281insTG
ENST00000706897.1:n.280_281insTG
ENST00000706898.1:c.4_5insTG	ENSP00000516611.1:p.Ala2ValfsTer19
ENST00000706899.1:n.280_281insTG
ENST00000706901.1:c.4_5insTG	ENSP00000516612.1:p.Ala2ValfsTer19
ENST00000706902.1:c.4_5insTG	ENSP00000516613.1:p.Ala2ValfsTer19
ENST00000706903.1:c.4_5insTG	ENSP00000516614.1:p.Ala2ValfsTer19
ENST00000706904.1:c.4_5insTG	ENSP00000516615.1:p.Ala2ValfsTer19
ENST00000706905.1:c.4_5insTG	ENSP00000516616.1:p.Ala2ValfsTer19
ENST00000376809.10:c.4_5insTG MANE Select	ENSP00000366005.5:p.Ala2ValfsTer19
ENST00000638375.1:c.4_5insTG	ENSP00000492789.1:p.Ala2ValfsTer19
ENST00000376802.2:c.4_5insTG	ENSP00000365998.2:p.Ala2ValfsTer19
ENST00000376806.9:c.4_5insTG	ENSP00000366002.5:p.Ala2ValfsTer19
ENST00000376809.9:c.4_5insTG	ENSP00000366005.5:p.Ala2ValfsTer19
ENST00000396634.5:c.4_5insTG	ENSP00000379873.1:p.Ala2ValfsTer19
ENST00000429656.1:n.511_512insAC
ENST00000461903.1:n.4_5insTG
ENST00000479320.5:n.4_5insTG
ENST00000495183.5:n.6_7insTG
ENST00000496081.5:n.10_11insTG
NM_002116.7:c.4_5insTG	NP_002107.3:p.Ala2ValfsTer19
NM_002116.8:c.4_5insTG MANE Select	NP_002107.3:p.Ala2ValfsTer19