Canonical Allele Identifier: CA2677798277

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945716-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945716A>C , CM000668.2:g.29945716A>C	GRCh38
NC_000006.11:g.29913493A>C , CM000668.1:g.29913493A>C	GRCh37
NC_000006.10:g.30021472A>C	NCBI36
NG_029217.2:g.8252A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1242A>C	ENSP00000492789.2:n.1242A>C
ENST00000706893.1:c.*343A>C	ENSP00000516609.1:n.*343A>C
ENST00000706894.1:c.*343A>C	ENSP00000516610.1:n.*343A>C
ENST00000706895.1:n.2348A>C
ENST00000706896.1:n.2655A>C
ENST00000706897.1:n.2077A>C
ENST00000706898.1:c.*261A>C	ENSP00000516611.1:n.*261A>C
ENST00000706899.1:n.2213A>C
ENST00000706900.1:c.*261A>C	ENSP00000516617.1:n.*261A>C
ENST00000706901.1:c.*261A>C	ENSP00000516612.1:n.*261A>C
ENST00000706902.1:c.1093+435A>C	ENSP00000516613.1:n.1093+435A>C
ENST00000706903.1:c.*124+137A>C	ENSP00000516614.1:n.*124+137A>C
ENST00000706904.1:c.1093+435A>C	ENSP00000516615.1:n.1093+435A>C
ENST00000706905.1:c.*261A>C	ENSP00000516616.1:n.*261A>C
ENST00000376809.10:c.*261A>C MANE Select	ENSP00000366005.5:n.*261A>C
ENST00000376802.2:c.*261A>C	ENSP00000365998.2:n.*261A>C
ENST00000376806.9:c.*261A>C	ENSP00000366002.5:n.*261A>C
ENST00000376809.9:c.*261A>C	ENSP00000366005.5:n.*261A>C
ENST00000396634.5:c.*261A>C	ENSP00000379873.1:n.*261A>C
ENST00000495183.5:n.1598A>C
ENST00000496081.5:n.1618A>C
NM_002116.7:c.*261A>C	NP_002107.3:n.*261A>C
NM_002116.8:c.*261A>C MANE Select	NP_002107.3:n.*261A>C