Canonical Allele Identifier: CA2677798041

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945644-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945644T>A , CM000668.2:g.29945644T>A	GRCh38
NC_000006.11:g.29913421T>A , CM000668.1:g.29913421T>A	GRCh37
NC_000006.10:g.30021400T>A	NCBI36
NG_029217.2:g.8180T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000638375.2:c.1170T>A	ENSP00000492789.2:n.1170T>A
ENST00000706892.1:n.2996T>A
ENST00000706893.1:c.*271T>A	ENSP00000516609.1:n.*271T>A
ENST00000706894.1:c.*271T>A	ENSP00000516610.1:n.*271T>A
ENST00000706895.1:n.2276T>A
ENST00000706896.1:n.2583T>A
ENST00000706897.1:n.2005T>A
ENST00000706898.1:c.*189T>A	ENSP00000516611.1:n.*189T>A
ENST00000706899.1:n.2141T>A
ENST00000706900.1:c.*189T>A	ENSP00000516617.1:n.*189T>A
ENST00000706901.1:c.*189T>A	ENSP00000516612.1:n.*189T>A
ENST00000706902.1:c.1093+363T>A	ENSP00000516613.1:n.1093+363T>A
ENST00000706903.1:c.*124+65T>A	ENSP00000516614.1:n.*124+65T>A
ENST00000706904.1:c.1093+363T>A	ENSP00000516615.1:n.1093+363T>A
ENST00000706905.1:c.*189T>A	ENSP00000516616.1:n.*189T>A
ENST00000376809.10:c.*189T>A MANE Select	ENSP00000366005.5:n.*189T>A
ENST00000376802.2:c.*189T>A	ENSP00000365998.2:n.*189T>A
ENST00000376806.9:c.*189T>A	ENSP00000366002.5:n.*189T>A
ENST00000376809.9:c.*189T>A	ENSP00000366005.5:n.*189T>A
ENST00000396634.5:c.*189T>A	ENSP00000379873.1:n.*189T>A
ENST00000495183.5:n.1526T>A
ENST00000496081.5:n.1546T>A
NM_002116.7:c.*189T>A	NP_002107.3:n.*189T>A
NM_002116.8:c.*189T>A MANE Select	NP_002107.3:n.*189T>A