Canonical Allele Identifier: CA449373428

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29942552-G-C
• MyVariant Identifiers: chr6:g.29910329G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29942552G>C , CM000668.2:g.29942552G>C	GRCh38
NC_000006.11:g.29910329G>C , CM000668.1:g.29910329G>C	GRCh37
NC_000006.10:g.30018308G>C	NCBI36
NG_029217.2:g.5087G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706892.1:n.275G>C
ENST00000706893.1:c.-2G>C	ENSP00000516609.1:n.-2G>C
ENST00000706894.1:c.-2G>C	ENSP00000516610.1:n.-2G>C
ENST00000706895.1:n.275G>C
ENST00000706896.1:n.275G>C
ENST00000706897.1:n.275G>C
ENST00000706898.1:c.-2G>C	ENSP00000516611.1:n.-2G>C
ENST00000706899.1:n.275G>C
ENST00000706901.1:c.-2G>C	ENSP00000516612.1:n.-2G>C
ENST00000706902.1:c.-2G>C	ENSP00000516613.1:n.-2G>C
ENST00000706903.1:c.-2G>C	ENSP00000516614.1:n.-2G>C
ENST00000706904.1:c.-2G>C	ENSP00000516615.1:n.-2G>C
ENST00000706905.1:c.-2G>C	ENSP00000516616.1:n.-2G>C
ENST00000376809.10:c.-2G>C MANE Select	ENSP00000366005.5:n.-2G>C
ENST00000376802.2:c.-2G>C	ENSP00000365998.2:n.-2G>C
ENST00000376806.9:c.-2G>C	ENSP00000366002.5:n.-2G>C
ENST00000376809.9:c.-2G>C	ENSP00000366005.5:n.-2G>C
ENST00000396634.5:c.-2G>C	ENSP00000379873.1:n.-2G>C
ENST00000429656.1:n.516C>G
ENST00000495183.5:n.1G>C
ENST00000496081.5:n.5G>C
NM_002116.7:c.-2G>C	NP_002107.3:n.-2G>C
NM_002116.8:c.-2G>C MANE Select	NP_002107.3:n.-2G>C