Canonical Allele Identifier: CA1618520781

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945496_29945498delinsCTG , CM000668.2:g.29945496_29945498delinsCTG	GRCh38
NC_000006.11:g.29913273_29913275delinsCTG , CM000668.1:g.29913273_29913275delinsCTG	GRCh37
NC_000006.10:g.30021252_30021254delinsCTG	NCBI36
NG_029217.2:g.8032_8034delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1022_1024delinsCTG	ENSP00000492789.2:n.1022_1024delinsCTG
ENST00000706892.1:n.2848_2850delinsCTG
ENST00000706893.1:c.*123_*125delinsCTG	ENSP00000516609.1:n.*123_*125delinsCTG
ENST00000706894.1:c.*123_*125delinsCTG	ENSP00000516610.1:n.*123_*125delinsCTG
ENST00000706895.1:n.2128_2130delinsCTG
ENST00000706896.1:n.2435_2437delinsCTG
ENST00000706897.1:n.1857_1859delinsCTG
ENST00000706898.1:c.*41_*43delinsCTG	ENSP00000516611.1:n.*41_*43delinsCTG
ENST00000706899.1:n.1993_1995delinsCTG
ENST00000706900.1:c.*41_*43delinsCTG	ENSP00000516617.1:n.*41_*43delinsCTG
ENST00000706901.1:c.*41_*43delinsCTG	ENSP00000516612.1:n.*41_*43delinsCTG
ENST00000706902.1:c.1093+215_1093+217delinsCTG	ENSP00000516613.1:n.1093+215_1093+217delinsCTG
ENST00000706903.1:c.*41_*43delinsCTG	ENSP00000516614.1:n.*41_*43delinsCTG
ENST00000706904.1:c.1093+215_1093+217delinsCTG	ENSP00000516615.1:n.1093+215_1093+217delinsCTG
ENST00000706905.1:c.*41_*43delinsCTG	ENSP00000516616.1:n.*41_*43delinsCTG
ENST00000376809.10:c.*41_*43delinsCTG MANE Select	ENSP00000366005.5:n.*41_*43delinsCTG
ENST00000376802.2:c.*41_*43delinsCTG	ENSP00000365998.2:n.*41_*43delinsCTG
ENST00000376806.9:c.*41_*43delinsCTG	ENSP00000366002.5:n.*41_*43delinsCTG
ENST00000376809.9:c.*41_*43delinsCTG	ENSP00000366005.5:n.*41_*43delinsCTG
ENST00000396634.5:c.*41_*43delinsCTG	ENSP00000379873.1:n.*41_*43delinsCTG
ENST00000495183.5:n.1378_1380delinsCTG
ENST00000496081.5:n.1398_1400delinsCTG
NM_002116.7:c.*41_*43delinsCTG	NP_002107.3:n.*41_*43delinsCTG
NM_002116.8:c.*41_*43delinsCTG MANE Select	NP_002107.3:n.*41_*43delinsCTG