Canonical Allele Identifier: CA449373296

Gene: HLA-A

Linked Data

• gnomAD v2: 6-29910318-C-T
• gnomAD v3: 6-29942541-C-T
• gnomAD v4: 6-29942541-C-T
• MyVariant Identifiers: chr6:g.29910318C>T (hg19) ; chr6:g.29910318_29910329delinsTCAGACGCCGAG (hg19) ; chr6:g.29942541_29942552delinsTCAGACGCCGAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29942541C>T , CM000668.2:g.29942541C>T	GRCh38
NC_000006.11:g.29910318C>T , CM000668.1:g.29910318C>T	GRCh37
NC_000006.10:g.30018297C>T	NCBI36
NG_029217.2:g.5076C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706892.1:n.264C>T
ENST00000706893.1:c.-13C>T	ENSP00000516609.1:n.-13C>T
ENST00000706894.1:c.-13C>T	ENSP00000516610.1:n.-13C>T
ENST00000706895.1:n.264C>T
ENST00000706896.1:n.264C>T
ENST00000706897.1:n.264C>T
ENST00000706898.1:c.-13C>T	ENSP00000516611.1:n.-13C>T
ENST00000706899.1:n.264C>T
ENST00000706901.1:c.-13C>T	ENSP00000516612.1:n.-13C>T
ENST00000706902.1:c.-13C>T	ENSP00000516613.1:n.-13C>T
ENST00000706903.1:c.-13C>T	ENSP00000516614.1:n.-13C>T
ENST00000706904.1:c.-13C>T	ENSP00000516615.1:n.-13C>T
ENST00000706905.1:c.-13C>T	ENSP00000516616.1:n.-13C>T
ENST00000376809.10:c.-13C>T MANE Select	ENSP00000366005.5:n.-13C>T
ENST00000376806.9:c.-13C>T	ENSP00000366002.5:n.-13C>T
ENST00000376809.9:c.-13C>T	ENSP00000366005.5:n.-13C>T
ENST00000396634.5:c.-13C>T	ENSP00000379873.1:n.-13C>T
ENST00000429656.1:n.527G>A
NM_002116.7:c.-13C>T	NP_002107.3:n.-13C>T
NM_002116.8:c.-13C>T MANE Select	NP_002107.3:n.-13C>T