Canonical Allele Identifier: CA823769986

Gene: HLA-A

Linked Data

• dbSNP Id: rs577937205
• gnomAD v3: 6-29945762-C-T
• gnomAD v4: 6-29945762-C-T
• MyVariant Identifiers: chr6:g.29913539C>T (hg19) ; chr6:g.29945762C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945762C>T , CM000668.2:g.29945762C>T	GRCh38
NC_000006.11:g.29913539C>T , CM000668.1:g.29913539C>T	GRCh37
NC_000006.10:g.30021518C>T	NCBI36
NG_029217.2:g.8298C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1288C>T	ENSP00000492789.2:n.1288C>T
ENST00000706895.1:n.2394C>T
ENST00000706896.1:n.2701C>T
ENST00000706897.1:n.2123C>T
ENST00000706898.1:c.*307C>T	ENSP00000516611.1:n.*307C>T
ENST00000706899.1:n.2259C>T
ENST00000706900.1:c.*307C>T	ENSP00000516617.1:n.*307C>T
ENST00000706901.1:c.*307C>T	ENSP00000516612.1:n.*307C>T
ENST00000706902.1:c.1093+481C>T	ENSP00000516613.1:n.1093+481C>T
ENST00000706903.1:c.*124+183C>T	ENSP00000516614.1:n.*124+183C>T
ENST00000706904.1:c.1093+481C>T	ENSP00000516615.1:n.1093+481C>T
ENST00000706905.1:c.*307C>T	ENSP00000516616.1:n.*307C>T
ENST00000376809.10:c.*307C>T MANE Select	ENSP00000366005.5:n.*307C>T
ENST00000376802.2:c.*307C>T	ENSP00000365998.2:n.*307C>T
ENST00000376806.9:c.*307C>T	ENSP00000366002.5:n.*307C>T
ENST00000376809.9:c.*307C>T	ENSP00000366005.5:n.*307C>T
ENST00000396634.5:c.*307C>T	ENSP00000379873.1:n.*307C>T
ENST00000495183.5:n.1644C>T
ENST00000496081.5:n.1664C>T
NM_002116.7:c.*307C>T	NP_002107.3:n.*307C>T
NM_002116.8:c.*307C>T MANE Select	NP_002107.3:n.*307C>T