Canonical Allele Identifier: CA2677798138

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945685-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945685G>T , CM000668.2:g.29945685G>T	GRCh38
NC_000006.11:g.29913462G>T , CM000668.1:g.29913462G>T	GRCh37
NC_000006.10:g.30021441G>T	NCBI36
NG_029217.2:g.8221G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1211G>T	ENSP00000492789.2:n.1211G>T
ENST00000706892.1:n.3037G>T
ENST00000706893.1:c.*312G>T	ENSP00000516609.1:n.*312G>T
ENST00000706894.1:c.*312G>T	ENSP00000516610.1:n.*312G>T
ENST00000706895.1:n.2317G>T
ENST00000706896.1:n.2624G>T
ENST00000706897.1:n.2046G>T
ENST00000706898.1:c.*230G>T	ENSP00000516611.1:n.*230G>T
ENST00000706899.1:n.2182G>T
ENST00000706900.1:c.*230G>T	ENSP00000516617.1:n.*230G>T
ENST00000706901.1:c.*230G>T	ENSP00000516612.1:n.*230G>T
ENST00000706902.1:c.1093+404G>T	ENSP00000516613.1:n.1093+404G>T
ENST00000706903.1:c.*124+106G>T	ENSP00000516614.1:n.*124+106G>T
ENST00000706904.1:c.1093+404G>T	ENSP00000516615.1:n.1093+404G>T
ENST00000706905.1:c.*230G>T	ENSP00000516616.1:n.*230G>T
ENST00000376809.10:c.*230G>T MANE Select	ENSP00000366005.5:n.*230G>T
ENST00000376802.2:c.*230G>T	ENSP00000365998.2:n.*230G>T
ENST00000376806.9:c.*230G>T	ENSP00000366002.5:n.*230G>T
ENST00000376809.9:c.*230G>T	ENSP00000366005.5:n.*230G>T
ENST00000396634.5:c.*230G>T	ENSP00000379873.1:n.*230G>T
ENST00000495183.5:n.1567G>T
ENST00000496081.5:n.1587G>T
NM_002116.7:c.*230G>T	NP_002107.3:n.*230G>T
NM_002116.8:c.*230G>T MANE Select	NP_002107.3:n.*230G>T