Canonical Allele Identifier: CA449461019

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29942782-C-T
• MyVariant Identifiers: chr6:g.29910559C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29942782C>T , CM000668.2:g.29942782C>T	GRCh38
NC_000006.11:g.29910559C>T , CM000668.1:g.29910559C>T	GRCh37
NC_000006.10:g.30018538C>T	NCBI36
NG_029217.2:g.5317C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000638375.2:c.99C>T	ENSP00000492789.2:p.Phe33=
ENST00000706892.1:n.375C>T
ENST00000706893.1:c.99C>T	ENSP00000516609.1:p.Phe33=
ENST00000706894.1:c.99C>T	ENSP00000516610.1:p.Phe33=
ENST00000706895.1:n.375C>T
ENST00000706896.1:n.375C>T
ENST00000706897.1:n.375C>T
ENST00000706898.1:c.99C>T	ENSP00000516611.1:p.Phe33=
ENST00000706899.1:n.375C>T
ENST00000706900.1:c.15C>T	ENSP00000516617.1:p.Phe5=
ENST00000706901.1:c.99C>T	ENSP00000516612.1:p.Phe33=
ENST00000706902.1:c.99C>T	ENSP00000516613.1:p.Phe33=
ENST00000706903.1:c.99C>T	ENSP00000516614.1:p.Phe33=
ENST00000706904.1:c.99C>T	ENSP00000516615.1:p.Phe33=
ENST00000706905.1:c.99C>T	ENSP00000516616.1:p.Phe33=
ENST00000376809.10:c.99C>T MANE Select	ENSP00000366005.5:p.Phe33=
ENST00000638375.1:c.99C>T	ENSP00000492789.1:p.Phe33=
ENST00000376802.2:c.99C>T	ENSP00000365998.2:p.Phe33=
ENST00000376806.9:c.99C>T	ENSP00000366002.5:p.Phe33=
ENST00000376809.9:c.99C>T	ENSP00000366005.5:p.Phe33=
ENST00000396634.5:c.99C>T	ENSP00000379873.1:p.Phe33=
ENST00000429656.1:n.286G>A
ENST00000461903.1:n.99C>T
ENST00000479320.5:n.99C>T
ENST00000495183.5:n.101C>T
ENST00000496081.5:n.105C>T
NM_002116.7:c.99C>T	NP_002107.3:p.Phe33=
NM_002116.8:c.99C>T MANE Select	NP_002107.3:p.Phe33=