Canonical Allele Identifier: CA3693758

Gene: HLA-A

Linked Data

• dbSNP Id: rs9260210
• ExAC: 6:29913192 G / T
• gnomAD v2: 6-29913192-G-T
• gnomAD v3: 6-29945415-G-T
• gnomAD v4: 6-29945415-G-T
• MyVariant Identifiers: chr6:g.29913192G>T (hg19) ; chr6:g.29945415G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945415G>T , CM000668.2:g.29945415G>T	GRCh38
NC_000006.11:g.29913192G>T , CM000668.1:g.29913192G>T	GRCh37
NC_000006.10:g.30021171G>T	NCBI36
NG_029217.2:g.7951G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000638375.2:c.977-36G>T	ENSP00000492789.2:n.977-36G>T
ENST00000706892.1:n.2767G>T
ENST00000706893.1:c.*78-36G>T	ENSP00000516609.1:n.*78-36G>T
ENST00000706894.1:c.*42G>T	ENSP00000516610.1:n.*42G>T
ENST00000706895.1:n.2047G>T
ENST00000706896.1:n.2390-36G>T
ENST00000706897.1:n.1812-36G>T
ENST00000706898.1:c.1112-36G>T	ENSP00000516611.1:n.1112-36G>T
ENST00000706899.1:n.1948-36G>T
ENST00000706900.1:c.1010-36G>T	ENSP00000516617.1:n.1010-36G>T
ENST00000706901.1:c.1094-36G>T	ENSP00000516612.1:n.1094-36G>T
ENST00000706902.1:c.1093+134G>T	ENSP00000516613.1:n.1093+134G>T
ENST00000706903.1:c.1094-36G>T	ENSP00000516614.1:n.1094-36G>T
ENST00000706904.1:c.1093+134G>T	ENSP00000516615.1:n.1093+134G>T
ENST00000706905.1:c.1094-36G>T	ENSP00000516616.1:n.1094-36G>T
ENST00000376809.10:c.1094-36G>T MANE Select	ENSP00000366005.5:n.1094-36G>T
ENST00000376802.2:c.896-36G>T	ENSP00000365998.2:n.896-36G>T
ENST00000376806.9:c.1112-36G>T	ENSP00000366002.5:n.1112-36G>T
ENST00000376809.9:c.1094-36G>T	ENSP00000366005.5:n.1094-36G>T
ENST00000396634.5:c.1094-36G>T	ENSP00000379873.1:n.1094-36G>T
ENST00000495183.5:n.1333-36G>T
ENST00000496081.5:n.1353-36G>T
NM_002116.7:c.1094-36G>T	NP_002107.3:n.1094-36G>T
NM_002116.8:c.1094-36G>T MANE Select	NP_002107.3:n.1094-36G>T