Canonical Allele Identifier: CA2677795435

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29944837-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944837C>T , CM000668.2:g.29944837C>T	GRCh38
NC_000006.11:g.29912614C>T , CM000668.1:g.29912614C>T	GRCh37
NC_000006.10:g.30020593C>T	NCBI36
NG_029217.2:g.7373C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000638375.2:c.896-222C>T	ENSP00000492789.2:n.896-222C>T
ENST00000706892.1:n.2189C>T
ENST00000706893.1:c.1064+203C>T	ENSP00000516609.1:n.1064+203C>T
ENST00000706894.1:c.1013-222C>T	ENSP00000516610.1:n.1013-222C>T
ENST00000706895.1:n.1611C>T
ENST00000706896.1:n.2087C>T
ENST00000706897.1:n.1509C>T
ENST00000706898.1:c.1030+203C>T	ENSP00000516611.1:n.1030+203C>T
ENST00000706899.1:n.1867-222C>T
ENST00000706900.1:c.929-222C>T	ENSP00000516617.1:n.929-222C>T
ENST00000706901.1:c.1013-222C>T	ENSP00000516612.1:n.1013-222C>T
ENST00000706902.1:c.1013-222C>T	ENSP00000516613.1:n.1013-222C>T
ENST00000706903.1:c.1013-222C>T	ENSP00000516614.1:n.1013-222C>T
ENST00000706904.1:c.1013-222C>T	ENSP00000516615.1:n.1013-222C>T
ENST00000706905.1:c.1013-222C>T	ENSP00000516616.1:n.1013-222C>T
ENST00000376809.10:c.1013-222C>T MANE Select	ENSP00000366005.5:n.1013-222C>T
ENST00000638375.1:c.896-222C>T	ENSP00000492789.1:n.896-222C>T
ENST00000376802.2:c.895+440C>T	ENSP00000365998.2:n.895+440C>T
ENST00000376806.9:c.1030+203C>T	ENSP00000366002.5:n.1030+203C>T
ENST00000376809.9:c.1013-222C>T	ENSP00000366005.5:n.1013-222C>T
ENST00000396634.5:c.1013-222C>T	ENSP00000379873.1:n.1013-222C>T
ENST00000461903.1:n.1271+203C>T
ENST00000479320.5:n.1254-222C>T
ENST00000495183.5:n.1255+221C>T
ENST00000496081.5:n.1050C>T
NM_002116.7:c.1013-222C>T	NP_002107.3:n.1013-222C>T
NM_002116.8:c.1013-222C>T MANE Select	NP_002107.3:n.1013-222C>T