Canonical Allele Identifier: CA2677798006

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945628-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945628T>C , CM000668.2:g.29945628T>C	GRCh38
NC_000006.11:g.29913405T>C , CM000668.1:g.29913405T>C	GRCh37
NC_000006.10:g.30021384T>C	NCBI36
NG_029217.2:g.8164T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1154T>C	ENSP00000492789.2:n.1154T>C
ENST00000706892.1:n.2980T>C
ENST00000706893.1:c.*255T>C	ENSP00000516609.1:n.*255T>C
ENST00000706894.1:c.*255T>C	ENSP00000516610.1:n.*255T>C
ENST00000706895.1:n.2260T>C
ENST00000706896.1:n.2567T>C
ENST00000706897.1:n.1989T>C
ENST00000706898.1:c.*173T>C	ENSP00000516611.1:n.*173T>C
ENST00000706899.1:n.2125T>C
ENST00000706900.1:c.*173T>C	ENSP00000516617.1:n.*173T>C
ENST00000706901.1:c.*173T>C	ENSP00000516612.1:n.*173T>C
ENST00000706902.1:c.1093+347T>C	ENSP00000516613.1:n.1093+347T>C
ENST00000706903.1:c.*124+49T>C	ENSP00000516614.1:n.*124+49T>C
ENST00000706904.1:c.1093+347T>C	ENSP00000516615.1:n.1093+347T>C
ENST00000706905.1:c.*173T>C	ENSP00000516616.1:n.*173T>C
ENST00000376809.10:c.*173T>C MANE Select	ENSP00000366005.5:n.*173T>C
ENST00000376802.2:c.*173T>C	ENSP00000365998.2:n.*173T>C
ENST00000376806.9:c.*173T>C	ENSP00000366002.5:n.*173T>C
ENST00000376809.9:c.*173T>C	ENSP00000366005.5:n.*173T>C
ENST00000396634.5:c.*173T>C	ENSP00000379873.1:n.*173T>C
ENST00000495183.5:n.1510T>C
ENST00000496081.5:n.1530T>C
NM_002116.7:c.*173T>C	NP_002107.3:n.*173T>C
NM_002116.8:c.*173T>C MANE Select	NP_002107.3:n.*173T>C