Canonical Allele Identifier: CA1618520816

Gene: HLA-A

Linked Data

• dbSNP Id: rs1582008192
• gnomAD v4: 6-29945516-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945516T>C , CM000668.2:g.29945516T>C	GRCh38
NC_000006.11:g.29913293T>C , CM000668.1:g.29913293T>C	GRCh37
NC_000006.10:g.30021272T>C	NCBI36
NG_029217.2:g.8052T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1042T>C	ENSP00000492789.2:n.1042T>C
ENST00000706892.1:n.2868T>C
ENST00000706893.1:c.*143T>C	ENSP00000516609.1:n.*143T>C
ENST00000706894.1:c.*143T>C	ENSP00000516610.1:n.*143T>C
ENST00000706895.1:n.2148T>C
ENST00000706896.1:n.2455T>C
ENST00000706897.1:n.1877T>C
ENST00000706898.1:c.*61T>C	ENSP00000516611.1:n.*61T>C
ENST00000706899.1:n.2013T>C
ENST00000706900.1:c.*61T>C	ENSP00000516617.1:n.*61T>C
ENST00000706901.1:c.*61T>C	ENSP00000516612.1:n.*61T>C
ENST00000706902.1:c.1093+235T>C	ENSP00000516613.1:n.1093+235T>C
ENST00000706903.1:c.*61T>C	ENSP00000516614.1:n.*61T>C
ENST00000706904.1:c.1093+235T>C	ENSP00000516615.1:n.1093+235T>C
ENST00000706905.1:c.*61T>C	ENSP00000516616.1:n.*61T>C
ENST00000376809.10:c.*61T>C MANE Select	ENSP00000366005.5:n.*61T>C
ENST00000376802.2:c.*61T>C	ENSP00000365998.2:n.*61T>C
ENST00000376806.9:c.*61T>C	ENSP00000366002.5:n.*61T>C
ENST00000376809.9:c.*61T>C	ENSP00000366005.5:n.*61T>C
ENST00000396634.5:c.*61T>C	ENSP00000379873.1:n.*61T>C
ENST00000495183.5:n.1398T>C
ENST00000496081.5:n.1418T>C
NM_002116.7:c.*61T>C	NP_002107.3:n.*61T>C
NM_002116.8:c.*61T>C MANE Select	NP_002107.3:n.*61T>C