Canonical Allele Identifier: CA2770466894

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29943810_29943811insACAG , CM000668.2:g.29943810_29943811insACAG	GRCh38
NC_000006.11:g.29911587_29911588insACAG , CM000668.1:g.29911587_29911588insACAG	GRCh37
NC_000006.10:g.30019566_30019567insACAG	NCBI36
NG_029217.2:g.6346_6347insACAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.619+267_619+268insACAG	ENSP00000492789.2:n.619+267_619+268insACAG
ENST00000706892.1:n.1162_1163insACAG
ENST00000706893.1:c.619+267_619+268insACAG	ENSP00000516609.1:n.619+267_619+268insACAG
ENST00000706894.1:c.619+267_619+268insACAG	ENSP00000516610.1:n.619+267_619+268insACAG
ENST00000706895.1:n.895+267_895+268insACAG
ENST00000706896.1:n.1162_1163insACAG
ENST00000706897.1:n.895+267_895+268insACAG
ENST00000706898.1:c.619+267_619+268insACAG	ENSP00000516611.1:n.619+267_619+268insACAG
ENST00000706899.1:n.1162_1163insACAG
ENST00000706900.1:c.535+267_535+268insACAG	ENSP00000516617.1:n.535+267_535+268insACAG
ENST00000706901.1:c.619+267_619+268insACAG	ENSP00000516612.1:n.619+267_619+268insACAG
ENST00000706902.1:c.619+267_619+268insACAG	ENSP00000516613.1:n.619+267_619+268insACAG
ENST00000706903.1:c.619+267_619+268insACAG	ENSP00000516614.1:n.619+267_619+268insACAG
ENST00000706904.1:c.619+267_619+268insACAG	ENSP00000516615.1:n.619+267_619+268insACAG
ENST00000706905.1:c.619+267_619+268insACAG	ENSP00000516616.1:n.619+267_619+268insACAG
ENST00000376809.10:c.619+267_619+268insACAG MANE Select	ENSP00000366005.5:n.619+267_619+268insACAG
ENST00000638375.1:c.619+267_619+268insACAG	ENSP00000492789.1:n.619+267_619+268insACAG
ENST00000376802.2:c.619+267_619+268insACAG	ENSP00000365998.2:n.619+267_619+268insACAG
ENST00000376806.9:c.619+267_619+268insACAG	ENSP00000366002.5:n.619+267_619+268insACAG
ENST00000376809.9:c.619+267_619+268insACAG	ENSP00000366005.5:n.619+267_619+268insACAG
ENST00000396634.5:c.619+267_619+268insACAG	ENSP00000379873.1:n.619+267_619+268insACAG
ENST00000461903.1:n.860+267_860+268insACAG
ENST00000479320.5:n.860+267_860+268insACAG
ENST00000495183.5:n.862+267_862+268insACAG
ENST00000496081.5:n.436+267_436+268insACAG
NM_002116.7:c.619+267_619+268insACAG	NP_002107.3:n.619+267_619+268insACAG
NM_002116.8:c.619+267_619+268insACAG MANE Select	NP_002107.3:n.619+267_619+268insACAG