Canonical Allele Identifier: CA1618519710

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944636_29944637delinsTG , CM000668.2:g.29944636_29944637delinsTG	GRCh38
NC_000006.11:g.29912413_29912414delinsTG , CM000668.1:g.29912413_29912414delinsTG	GRCh37
NC_000006.10:g.30020392_30020393delinsTG	NCBI36
NG_029217.2:g.7172_7173delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.895+239_895+240delinsTG	ENSP00000492789.2:n.895+239_895+240delinsTG
ENST00000706892.1:n.1988_1989delinsTG
ENST00000706893.1:c.1064+2_1064+3delinsTG	ENSP00000516609.1:n.1064+2_1064+3delinsTG
ENST00000706894.1:c.1012+20_1012+21delinsTG	ENSP00000516610.1:n.1012+20_1012+21delinsTG
ENST00000706895.1:n.1410_1411delinsTG
ENST00000706896.1:n.1886_1887delinsTG
ENST00000706897.1:n.1308_1309delinsTG
ENST00000706898.1:c.1030+2_1030+3delinsTG	ENSP00000516611.1:n.1030+2_1030+3delinsTG
ENST00000706899.1:n.1866+20_1866+21delinsTG
ENST00000706900.1:c.928+20_928+21delinsTG	ENSP00000516617.1:n.928+20_928+21delinsTG
ENST00000706901.1:c.1012+20_1012+21delinsTG	ENSP00000516612.1:n.1012+20_1012+21delinsTG
ENST00000706902.1:c.1012+20_1012+21delinsTG	ENSP00000516613.1:n.1012+20_1012+21delinsTG
ENST00000706903.1:c.1012+20_1012+21delinsTG	ENSP00000516614.1:n.1012+20_1012+21delinsTG
ENST00000706904.1:c.1012+20_1012+21delinsTG	ENSP00000516615.1:n.1012+20_1012+21delinsTG
ENST00000706905.1:c.1012+20_1012+21delinsTG	ENSP00000516616.1:n.1012+20_1012+21delinsTG
ENST00000376809.10:c.1012+20_1012+21delinsTG MANE Select	ENSP00000366005.5:n.1012+20_1012+21delinsTG
ENST00000638375.1:c.895+239_895+240delinsTG	ENSP00000492789.1:n.895+239_895+240delinsTG
ENST00000376802.2:c.895+239_895+240delinsTG	ENSP00000365998.2:n.895+239_895+240delinsTG
ENST00000376806.9:c.1030+2_1030+3delinsTG	ENSP00000366002.5:n.1030+2_1030+3delinsTG
ENST00000376809.9:c.1012+20_1012+21delinsTG	ENSP00000366005.5:n.1012+20_1012+21delinsTG
ENST00000396634.5:c.1012+20_1012+21delinsTG	ENSP00000379873.1:n.1012+20_1012+21delinsTG
ENST00000461903.1:n.1271+2_1271+3delinsTG
ENST00000479320.5:n.1253+20_1253+21delinsTG
ENST00000495183.5:n.1255+20_1255+21delinsTG
ENST00000496081.5:n.849_850delinsTG
NM_002116.7:c.1012+20_1012+21delinsTG	NP_002107.3:n.1012+20_1012+21delinsTG
NM_002116.8:c.1012+20_1012+21delinsTG MANE Select	NP_002107.3:n.1012+20_1012+21delinsTG